| 1 |
Partly verified |
Full text not readStored summary read |
N01 · Efficacy comparison and presentation of stored materialWhich existing values are recorded for the caries-prevention question?Required |
The selected existing question is 'prevention of incident caries', with original grade ? and note 'not measured'. Parent C50, Good and S/R1/I1/E+/B2 are context from the existing white-spot remineralization verdict; subclaim score, status and axes are absent. |
Record from the stored summary. Some information is in the stored summary. No new caries-prevention grade/effect is created and parent values are not inherited. Review of the existing content remains incomplete. |
Distinguish subclaim grade ?, note and missing score/status/axes from parent C50/axes |
Proposed follow-up material linking "Distinguish subclaim grade ?, note and missing score/status/axes from parent C50/axes" as a separate item; no new investigation, calculation or trial is performed in this work. |
| 2 |
Unverified |
Full text not readStored summary read |
N02 · Efficacy comparison and presentation of stored materialWas incident caries actually measured?Required |
The existing note and counterview say reductions in new caries/filling treatment were not measured. This is not changed into 0 events, confirmed prevention or a numerical finding of no effect. |
Record from the stored summary. Currently needed information is unverified. Direct caries definitions, events/denominators, observation windows and between-group effects/intervals are absent or unverified. Review of the existing content remains incomplete. |
Distinguish incident caries/new clinical events from existing lesion scores |
Proposed follow-up material linking "Distinguish incident caries/new clinical events from existing lesion scores" as a separate item; no new investigation, calculation or trial is performed in this work. |
| 3 |
Partly verified |
Full text not readStored summary read |
N03 · Efficacy comparison and presentation of stored materialIs existing white-spot ICDAS change the same as prevention of new caries?Required |
The original endpoint is the six-month ICDAS white-spot score, where higher is worse. Decreases in existing lesion scores are not transferred into incident-caries rates, fillings/pain or improved daily functioning. |
Record from the stored summary. Some information is in the stored summary. New lesion/caries events, individual links to progression/recovery of existing lesions and clinical-event results remain unverified. Review of the existing content remains incomplete. |
Existing lesions/visible remineralization, ICDAS and new events |
Proposed follow-up material linking "Existing lesions/visible remineralization, ICDAS and new events" as a separate item; no new investigation, calculation or trial is performed in this work. |
| 4 |
Partly verified |
Full text not readStored summary read |
N04 · Efficacy comparison and presentation of stored materialWhat outcome scope do ICDAS change values and P describe?Required |
The original ICDAS reduction of 0.80 versus 0.39 points, with between-group P=.003, is the original lesion-score result. It is not changed into a caries-prevention rate, independent-living/patient responder proportion or new between-group difference/CI. |
Record from the stored summary. Some information is in the stored summary. Group/lesion denominators, models, exact CIs and prespecified importance remain unverified. Review of the existing content remains incomplete. |
Original 0.80/0.39 points, P=.003 and lower-is-better direction |
Proposed follow-up material linking "Original 0.80/0.39 points, P=.003 and lower-is-better direction" as a separate item; no new investigation, calculation or trial is performed in this work. |
| 5 |
Partly verified |
Full text not readStored summary read |
N05 · Efficacy comparison and presentation of stored materialHow are baseline/six-month scores and the original change difference retained?Required |
The existing Korean verdict rationale's mousse 1.80→1.00, control 1.92→1.53 and change difference of 0.41 points are retained. No new reductions/differences are calculated from scores or converted into caries incidence. |
Record from the stored summary. Some information is in the stored summary. Analysis populations, adjustment/rounding, intervals and scale aggregation details for scores/change differences remain unverified. Review of the existing content remains incomplete. |
Roles of 1.80→1.00, 1.92→1.53 and the original 0.41 difference |
Proposed follow-up material linking "Roles of 1.80→1.00, 1.92→1.53 and the original 0.41 difference" as a separate item; no new investigation, calculation or trial is performed in this work. |
| 6 |
Unverified |
Full text not readStored summary read |
N06 · Efficacy comparison and presentation of stored materialDoes a clinically important minimum difference mean caries prevention?Required |
Statistical ICDAS change and original parent C50 are historical surrogate-outcome context. Neither 0.41 points nor P is used as a prespecified important difference, new caries-prevention effect or individual target. |
Record from the stored summary. Currently needed information is unverified. Prespecified ICDAS importance, between-group CIs and validated links to clinical events remain unverified. Review of the existing content remains incomplete. |
Distinguish lesion-score importance, direct clinical events and between-group intervals |
Proposed follow-up material linking "Distinguish lesion-score importance, direct clinical events and between-group intervals" as a separate item; no new investigation, calculation or trial is performed in this work. |
| 7 |
Unverified |
Full text not readStored summary read |
N07 · Efficacy comparison and presentation of stored materialWere filling treatment, pain or oral daily-life outcomes reported?Required |
The existing counterview records that reduced filling treatment was not measured. Wording that visible remineralization may be useful is not turned into numerical pain, chewing/daily-life improvement or actual treatment reduction. |
Record from the stored summary. Currently needed information is unverified. Direct filling/treatment, pain/oral daily-life scales, denominators/periods and between-group values remain unverified. Review of the existing content remains incomplete. |
Filling treatment/oral function, appearance assessment and new clinical outcomes |
Proposed follow-up material linking "Filling treatment/oral function, appearance assessment and new clinical outcomes" as a separate item; no new investigation, calculation or trial is performed in this work. |
| 8 |
Partly verified |
Full text not readStored summary read |
N08 · Efficacy comparison and presentation of stored materialWhich patients after orthodontic treatment were included?Required |
The original population has white spots after orthodontic treatment, and the existing English research account describes adolescents. This is not extended to all ages/teeth, general caries prevention or populations with other conditions. |
Record from the stored summary. Some information is in the stored summary. Exact ages, eligibility, orthodontic/baseline lesions, oral risk, comorbidities and recruitment conditions remain unverified. Review of the existing content remains incomplete. |
Post-orthodontic white spots, original English adolescent description and eligibility/baseline scope |
Proposed follow-up material linking "Post-orthodontic white spots, original English adolescent description and eligibility/baseline scope" as a separate item; no new investigation, calculation or trial is performed in this work. |
| 9 |
Partly verified |
Full text not readStored summary read |
N09 · Efficacy comparison and presentation of stored materialAre the original F-ACP components the same as other product families?Required |
Original F-ACP is an amorphous calcium-phosphate complex containing fluoride and carbonate. Fluoride/CPP-ACP in the original product-distribution wording is not reused as the same composition or preventive effect as this F-ACP. |
Record from the stored summary. Some information is in the stored summary. Exact concentrations, product identity, lots/manufacturing, formulation equivalence and direct material for other products remain unverified. Review of the existing content remains incomplete. |
Fluoride/carbonate-containing amorphous calcium phosphate and boundaries with CPP-ACP/fluoride products |
Proposed follow-up material linking "Fluoride/carbonate-containing amorphous calcium phosphate and boundaries with CPP-ACP/fluoride products" as a separate item; no new investigation, calculation or trial is performed in this work. |
| 10 |
Partly verified |
Full text not readStored summary read |
N10 · Efficacy comparison and presentation of stored materialWhat historical research conditions did the Essix retainer and six-month exposure describe?Required |
The original trial applied mousse in an Essix retainer for six months. This exposure is not changed into amounts/frequency, implementation/suitability instructions or product recommendations. |
Record from the stored summary. Some information is in the stored summary. Actual amounts/frequency, adherence/crossover, group exposure/concomitant care and control-management details remain unverified. Review of the existing content remains incomplete. |
Original mousse in a retainer, actual exposure/adherence and control |
Proposed follow-up material linking "Original mousse in a retainer, actual exposure/adherence and control" as a separate item; no new investigation, calculation or trial is performed in this work. |
| 11 |
Unverified |
Full text not readStored summary read |
N11 · Efficacy comparison and presentation of stored materialWhat did the control group receive?Required |
The original material contains control scores and a randomized controlled design, but absent exact control composition, appliance or oral care is not filled in. No treatment, appliance alone or an equivalent-fluoride control is not assumed. |
Record from the stored summary. Currently needed information is unverified. Control formulations, common/group care, fluoride/toothpaste/other exposures and blinding remain unverified. Review of the existing content remains incomplete. |
Mousse-control composition/appliance, common care and placebo definition |
Proposed follow-up material linking "Mousse-control composition/appliance, common care and placebo definition" as a separate item; no new investigation, calculation or trial is performed in this work. |
| 12 |
Partly verified |
Full text not readStored summary read |
N12 · Efficacy comparison and presentation of stored materialWhat is known about allocation and assessor blinding in the randomized design?Required |
The original is a randomized controlled trial. Its original B2 axis or randomized label is not inherited as verification of allocation concealment, patient/assessor blinding or clinical caries-event adjudication. |
Record from the stored summary. Some information is in the stored summary. Allocation/concealment, assessors, ICDAS measurement/photographs and blinding/awareness details remain unverified. Review of the existing content remains incomplete. |
Allocation-sequence generation/concealment and measurement of ICDAS/caries events |
Proposed follow-up material linking "Allocation-sequence generation/concealment and measurement of ICDAS/caries events" as a separate item; no new investigation, calculation or trial is performed in this work. |
| 13 |
Partly verified |
Full text not readStored summary read |
N13 · Efficacy comparison and presentation of stored materialWhat are the denominators of 106 randomized, 91 completers and 52/39?Required |
106 randomized, 91 completers (mousse 52/control 39) and original attrition of 14.2% are retained. No new dropout counts/rates, caries-observed participants per group or event denominators are calculated. |
Record from the stored summary. Some information is in the stored summary. Group follow-up, exclusions, dropout reasons, unmeasured clinical events and missing-data responses remain unverified. Review of the existing content remains incomplete. |
Distinguish randomized/completer populations, group denominators and original 14.2% attrition |
Proposed follow-up material linking "Distinguish randomized/completer populations, group denominators and original 14.2% attrition" as a separate item; no new investigation, calculation or trial is performed in this work. |
| 14 |
Partly verified |
Full text not readStored summary read |
N14 · Efficacy comparison and presentation of stored materialCan completer analysis describe effects in everyone randomized?Required |
The original account describes 91/106 completer analysis as a limitation. Completer ICDAS values are not extended to caries-prevention effects in all 106 participants, no missing data or complete follow-up. |
Record from the stored summary. Some information is in the stored summary. ITT/missing-data handling, sensitivity analyses, discontinuers' outcomes and prespecified plans remain unverified. Review of the existing content remains incomplete. |
Scope of original completers, ITT/missing-data plans and baseline/within-group selection |
Proposed follow-up material linking "Scope of original completers, ITT/missing-data plans and baseline/within-group selection" as a separate item; no new investigation, calculation or trial is performed in this work. |
| 15 |
Partly verified |
Full text not readStored summary read |
N15 · Efficacy comparison and presentation of stored materialAre people, teeth, lesions and repeated measurements the same units?Required |
Original 106/91 and 52/39 are person denominators. How ICDAS was aggregated by tooth/lesion is unknown; each tooth/time point is not counted as a new participant/independent trial. |
Record from the stored summary. Some information is in the stored summary. Lesion/tooth counts, within-person correlation, measurement/analysis models and group/time-point denominators remain unverified. Review of the existing content remains incomplete. |
Distinguish patient denominators, ICDAS aggregation/lesions and repeated-measure correlations |
Proposed follow-up material linking "Distinguish patient denominators, ICDAS aggregation/lesions and repeated-measure correlations" as a separate item; no new investigation, calculation or trial is performed in this work. |
| 16 |
Unverified |
Full text not readStored summary read |
N16 · Efficacy comparison and presentation of stored materialWhat are the actual observation windows for six-month ICDAS and caries incidence?Required |
The original trial period/ICDAS assessment is six months. It is not labeled as 0 caries events or prevention during that period, persistence afterward or confirmed long-term prevention. |
Record from the stored summary. Currently needed information is unverified. Caries observation/adjudication windows, long-term follow-up, events/missing data and periods after exposure ends remain unverified. Review of the existing content remains incomplete. |
Original six-month surrogate outcome and clinical-event periods/follow-up |
Proposed follow-up material linking "Original six-month surrogate outcome and clinical-event periods/follow-up" as a separate item; no new investigation, calculation or trial is performed in this work. |
| 17 |
Partly verified |
Full text not readStored summary read |
N17 · Efficacy comparison and presentation of stored materialWhat prespecified endpoint hierarchy included ICDAS and caries events?Required |
The existing evidence-list endpoint is six-month ICDAS. Unmeasured caries events are not turned into a primary time point, confirmatory endpoint, prespecified comparison or responder analysis. |
Record from the stored summary. Some information is in the stored summary. Protocols/SAPs, score/clinical-event plans, multiplicity and prespecified importance remain unverified. Review of the existing content remains incomplete. |
Original lesion-score endpoint, unmeasured caries and prespecified plans/multiplicity |
Proposed follow-up material linking "Original lesion-score endpoint, unmeasured caries and prespecified plans/multiplicity" as a separate item; no new investigation, calculation or trial is performed in this work. |
| 18 |
Partly verified |
Full text not readStored summary read |
N18 · Efficacy comparison and presentation of stored materialAre the same report, sibling remineralization question and population kept separate from independent totals?Required |
The parent/sibling ICDAS question and this caries-prevention question share the same Ciribè2024 report/population. Teeth/lesions, time points, scores/safety and the two questions are not added as new independent trials or total participants. |
Record from the stored summary. Some information is in the stored summary. Unique clinical trial/participant and independent-replication totals have not been verified and are not recorded. Review of the existing content remains incomplete. |
Ciribè2024, 106/91 participants and shared lesion/caries questions |
Proposed follow-up material linking "Ciribè2024, 106/91 participants and shared lesion/caries questions" as a separate item; no new investigation, calculation or trial is performed in this work. |
| 19 |
Partly verified |
Full text not readStored summary read |
N19 · Efficacy comparison and presentation of stored materialAre no external funding and unverified product provision/COI the same?Required |
The original funding account says no external funding was received and product-provision wording was not identified in publicly checked COI/acknowledgment text. External full text was not read in this work; this is not changed into no free product support or no company, employee or COI involvement. |
Record from the stored summary. Some information is in the stored summary. Institutional funding, products/manufacturers, employee authors, research/writing contributions, COI and supply agreements remain unverified. Review of the existing content remains incomplete. |
Original no-external-funding statement, unidentified products in the publicly checked scope and actual roles |
Proposed follow-up material linking "Original no-external-funding statement, unidentified products in the publicly checked scope and actual roles" as a separate item; no new investigation, calculation or trial is performed in this work. |
| 20 |
Partly verified |
Full text not readStored summary read |
N20 · Efficacy comparison and presentation of stored materialDoes 'registration not identified' verify actual absence?Required |
The original registration-identifier record says 'not identified'; the actual identifier remains unrecorded. This is not changed into a confirmed number, absence of registration or absence of a prespecified caries plan. |
Record from the stored summary. Some information is in the stored summary. Registration texts/changes, protocols/SAPs and endpoint/missing-data plans have not been read or accessed. Review of the existing content remains incomplete. |
Original registration-identifier record, unrecorded identifier and unread registration/protocol/SAP |
Proposed follow-up material linking "Original registration-identifier record, unrecorded identifier and unread registration/protocol/SAP" as a separate item; no new investigation, calculation or trial is performed in this work. |
| 21 |
Partly verified |
Full text not readStored summary read |
N21 · Harm-information gaps supplementing the efficacy tableWhat collection scope underlies six-month non-reporting of adverse effects?Supplementary |
The original safety wording says no adverse effects were reported by patients or caregivers over six months. The original Good label is not extended to overall zero risk, all patients, other products, long-term safety or use recommendations. |
Record from the stored summary. Some information is in the stored summary. Collection/questions, safety denominators, discontinuers/exposure, verification, severity/CIs and long-term/vulnerable-group harms remain unverified. Review of the existing content remains incomplete. |
Patient/caregiver reports, denominators/time and distinction from zero risk |
Proposed follow-up material linking "Patient/caregiver reports, denominators/time and distinction from zero risk" as a separate item; no new investigation, calculation or trial is performed in this work. |
| 22 |
Partly verified |
Full text not readStored summary read |
N22 · Efficacy comparison and presentation of stored materialDo sales/recommendation or other-product/population statements establish caries prevention?Required |
The original domestic distribution/recommendation wording is retained in the complete existing review summary. No new verification of current sales/recommendations, effects of all CPP-ACP/fluoride products or guidance on product selection, use, suitability, prevention or treatment is written. |
Record from the stored summary. Some information is in the stored summary. New verification of other compositions/populations, long-term caries/daily-life clinical outcomes and current distribution is outside scope or unverified. Review of the existing content remains incomplete. |
Original distribution history, this F-ACP surrogate outcome and direct material outside the scope |
Proposed follow-up material linking "Original distribution history, this F-ACP surrogate outcome and direct material outside the scope" as a separate item; no new investigation, calculation or trial is performed in this work. |
| 23 |
Partly verified |
Full text not readStored summary read |
N23 · Efficacy comparison and presentation of stored materialWhat was actually read from the stored summary, external papers and linked material?Required |
The complete stored summary was read for production and labeled 'summary read', with the original URL retained. External papers, registration, plans and COI material remain 'not read'; past review descriptions/bibliography alone do not raise the reading status in this work. |
Record from the stored summary. Some information is in the stored summary. External access, abstracts/full text, source comparison and external link/click tests were not performed. Review of the existing content remains incomplete. |
Stored summary, PMID38927409 URL and unread registration/plans/COI |
Proposed follow-up material linking "Stored summary, PMID38927409 URL and unread registration/plans/COI" as a separate item; no new investigation, calculation or trial is performed in this work. |
| 24 |
Partly verified |
Full text not readStored summary read |
N24 · Efficacy comparison and presentation of stored materialHow are existing Korean/English texts, grade ?/C50, dates, corrections and empty values retained?Required |
The complete review summary's Korean/English texts, parent C50/Good, unrecorded precision/false, empty corrections/deliberation and 2026-08-26 are retained. Selected grade ?/note and absent score/status/axes are distinguished from original limitation checks/cross-check history. |
Record from the stored summary. Some information is in the stored summary. No source/translation review, new verdict/correction or external update was performed in this existing record. Review of the existing content remains incomplete. |
Selected grade ?/note, parent C50/Good, null/false and 2026-08-26 |
Proposed follow-up material linking "Selected grade ?/note, parent C50/Good, null/false and 2026-08-26" as a separate item; no new investigation, calculation or trial is performed in this work. |
| 25 |
Partly verified |
Full text not readStored summary read |
N25 · Efficacy comparison and presentation of stored materialHow are condition preservation, case production and content review distinguished?Required |
Condition preservation, freezing, application, case production and content review are separate records. Review of the existing content is incomplete; record counts are not totals of unique clinical trials/participants. |
Record from the stored summary. Some information is in the stored summary. Review of the existing content is incomplete and clinical source material was not newly verified. Review of the existing content remains incomplete. |
Condition preservation, freezing, application, case production and incomplete content review |
Proposed follow-up material linking "Condition preservation, freezing, application, case production and incomplete content review" as a separate item; no new investigation, calculation or trial is performed in this work. |