CHAMGAP
VERIFIEDPassed the Codex final verification and publication gate. Evidence-verification cutoff: 2026-07-24. AI was used for research and drafting; the existence of all 2 cited sources was verified at the original page, followed by blind grading, adversarial audit, and build validation. Methodology v1.0.
Verdict No. 1814 · Search date 2026-07-24 · Methodology v1.0

Home narrowband UV-B,
does it really help with Control of psoriasis lesions and improvement of dermatology-related quality of life?

30-Second Summary
C
Evidence Grade C · 56 · Safety caution
Prescribed, supported home narrowband UV-B is generally noninferior to office phototherapy
Erythema, burns, blistering, itching, and cumulative ultraviolet exposure can occur. Photosensitizing medicines or disorders, prior skin cancer, and high cumulative exposure require dermatology assessment and monitoring.
What the
research shows
Home narrowband UV-B is rated C for psoriasis effectiveness compared with office narrowband UV-B. LITE randomized and analyzed 783 patients by intention to treat. At 12 weeks, coprimary PGA 0 or 1 response was 32.8% versus 25.6%, and DLQI of 5 or lower was 52.4% versus 33.6%; both met the prespecified -15% noninferiority margin. However, the trial used a noninferiority design and only an active office-based comparator without placebo. These are two bias defects, B2, capping the grade at C.
What the
ads claim
A device emitting narrowband UV-B around 311 to 313 nm is a physical fact, while psoriasis benefit is a clinical claim. The evidence supports prescribed home delivery with dosing locks and education as generally noninferior to office delivery, not arbitrary use of a cosmetic ultraviolet lamp.
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Useful facts when choosing a product

  • The LITE home unit was a Daavlin 7-series eight-bulb narrowband UV-B device using prescription protocols and treatment-frequency limits. It is not equivalent to a generic cosmetic ultraviolet lamp.
  • verdict 1815, which is C with 54 points, concerns guselkumab, a biologic drug compared with placebo; this verdict concerns home versus office delivery of phototherapy.
  • Existing drug verdicts also differ: verdict 1342, which is B with 76 points, concerns secukinumab, while verdict 1796, which is C with 56 points, concerns deucravacitinib.
ID

Chamgap Semantic Classification Code

Candidate index · review held

P.home-narrowband-uv-b-phototherapy.device.control-of-psoriasis-lesions-and-improvement-of-dermatology-related-quality-of-life.improve.active

Procedures, devices and tests > Home narrowband UV-B phototherapy > Device delivered > Control of psoriasis lesions and improvement of dermatology-related quality of life > Improvement claim > Active comparator

An automated migration candidate, not an issued permanent code; exact claim scope remains under review. This machine-generated migration candidate helps retrieval but is not a permanent assignment. The original verdict ID and URL remain authoritative.

Download semantic index (JSON) · Codebook v1

Gap Measurement · Verdict 1814 · C 56
What advertising claims
What independent, higher-quality research supports
△ GAP
01

What the research actually shows

Gelfand's LITE trial assigned 783 plaque or guttate psoriasis patients to home, 393, or office treatment, 390, and analyzed all 783 by intention to treat with missing outcomes counted as failures. At 12 weeks, PGA 0 or 1 occurred in 129 of 393 versus 100 of 390 and DLQI of 5 or lower in 206 of 393 versus 131 of 390; lower confidence bounds exceeded the prespecified -15% margin for both coprimary endpoints. Koek's PLUTO trial randomized 196, 98 per arm. Actual SAPASI50 analysis included 185, 94 and 91, and PASI50 analysis 175, 91 and 84. SAPASI50 difference 2.8% (95% CI -8.6 to 14.2) passed, while PASI50 -2.3% (-15.7 to 11.1) narrowly missed.

02

Why this is classified as C (56)

P, R2, I2, and E+ are present, and both LITE coprimary endpoints succeeded. Noninferiority and active-control-only design are two defects, B2, giving C with 56 points.

Counterpoint. Home treatment in these trials included prescription, education, skin-response dose adjustment, and use limits. Unsupervised self-irradiation is not the tested intervention.

Rejudgment record. Cross-check applied — Accepted successful PGA and DLQI coprimary noninferiority in all 783 LITE participants and broadly consistent PLUTO evidence, while recording the 15% noninferiority design and narrow PLUTO PASI50 miss

Stored scoring profile
EndpointPSymptom or function itself is the target - including patient reports and performance tests
ReplicationR2Independently replicated across trials
IndependenceI2Decisive evidence is publicly or non-profit funded
Effect sizeE+Meets the clinically important threshold

Stored derived and displayed grades match; this is not a current recalculation or validity check (C).

Sub-claim grades by effect

This ingredient is marketed for several effects. A single overall grade blends strong and weak claims together, so each effect is graded separately here. The overall grade reflects the strongest disconfirming or core claim.

Effect (sub-claim)GradeBasis
Achievement of PGA 0 or 1 with home treatmentCThe LITE coprimary endpoint was noninferior to office treatment.
Achievement of DLQI 5 or lower with home treatmentCThe patient-reported treatment-target coprimary endpoint was noninferior.
Achievement of PASI50 with home treatmentCThe PLUTO physician-assessed lower confidence bound missed the prespecified margin by 0.7 percentage point.

Cross-check — AI research and Codex final gate

AI was used for research and drafting. Blind grading, adversarial audit, and the methodology boundary rules were then reapplied before Codex performed the final evidence, grade, copy, and build checks. If a grade cannot be narrowed, both evidence positions and their reasons are published.
03

Evidence Table

StudyDesignSampleFundingEndpointResultWeight
Gelfand JM et al. 2024 LITEOpen-label multicenter pragmatic randomized noninferiority active-controlled trial783 randomized (393/390); actual primary intention-to-treat analysis 783Patient-Centered Outcomes Research Institute funding; Daavlin supplied devices, shipping, and optional education but had no research roleCoprimary week-12 PGA 0 or 1 and DLQI 5 or lower; noninferiority margin -15%32.8% versus 25.6% and 52.4% versus 33.6%; both coprimary noninferiority endpoints met.Pivotal large pragmatic trial
Koek MBG et al. 2009 PLUTOMulticenter pragmatic randomized single-blind noninferiority active-controlled trial196 randomized (98/98); SAPASI50 analysis 185 (94/91), PASI50 analysis 175 (91/84)Public Netherlands Organisation for Health Research and Development fundingPASI50 and SAPASI50; noninferiority margin -15%SAPASI50 met noninferiority, but the PASI50 lower bound of -15.7% missed the margin by 0.7 percentage point.Independent replication with one borderline coprimary measure miss
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Receipt — 2 References

All 2 cited sources were verified for existence at the original page (as of 2026-07-24).

Gelfand JM, Armstrong AW, Lim HW, et al. Home- vs Office-Based Narrowband UV-B Phototherapy for Patients With Psoriasis: The LITE Randomized Clinical Trial. JAMA Dermatol. 2024;160(12):1320-1328. PMID: 39319513. DOI: 10.1001/jamadermatol.2024.3897.
checked
Koek MBG, Buskens E, van Weelden H, et al. Home versus outpatient ultraviolet B phototherapy for mild to severe psoriasis: pragmatic multicentre randomised controlled non-inferiority trial (PLUTO study). BMJ. 2009;338:b1542. PMID: 19423623. DOI: 10.1136/bmj.b1542.
checked
Research and draft: AI used · Cross-check: blind grading and adversarial audit
Final verification and publication gate: Codex · Evidence date: 2026-07-24 · Corrections: none

Cite this verdict

Home narrowband UV-B x psoriasis control and quality-of-life improvement Evidence Grade C card
[Chamgap] Home narrowband UV-B x psoriasis control and quality-of-life improvement — Evidence Grade C·56. 2 cited sources checked. Source: https://chamgap.com/en/verdicts/skin-hair/home-narrowband-uvb-psoriasis-effectiveness-quality-of-life/ · CC BY 4.0

CC BY 4.0 — free to use with attribution; do not distort grades, numbers, or verdict meaning.

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What this document does and does not do

Chamgap is an information source. It reports what research has and has not confirmed; it does not tell readers what to take or buy. That decision belongs to readers and, when needed, medical or legal professionals. This verdict reflects literature available up to the search date and may change as new research appears. Nothing here is medical advice.