CHAMGAP
VERIFIEDPassed the Codex final verification and publication gate. Evidence-verification cutoff: 2026-08-26. AI was used for research and drafting; the existence of all 1 cited sources was verified at the original page, followed by blind grading, adversarial audit, and build validation. Methodology v0.8.
Verdict No. 2956 · Search date 2026-08-26 · Methodology v0.8

Olistic Women drinkable multi-ingredient nutraceutical,
does it really help with Increased TrichoScan hair density in premenopausal women with telogen effluvium?

30-Second Summary
C
Evidence Grade C · 50 · Safety unknown
Olistic Women increased six-month TrichoScan hair density, but evidence is limited to one small manufacturer trial
The authors explicitly stated that minor adverse events were not collected. This trial therefore cannot establish safety.
What the
research shows
Grade C. In a 106-participant double-blind trial, the day-180 increase in hair density was +27.31±2.61 versus +18.23±2.98 hairs/cm² with placebo (P<.01). This was hair counted by TrichoScan, not a patient-centered judgment that hair visibly looked fuller.
What the
ads claim
Women's hair supplements differ in formulation, ingredients, and populations. This result must not be extended to Viviscal, Nutrafol, or the entire supplement class.
*

Useful facts when choosing a product

  • The tested finished product was one 25-mL Olistic Women vial daily for six months.
  • The primary endpoint was hairs/cm² counted by TrichoScan, not appearance or satisfaction.
  • The trial was registered after primary completion.
Gap Measurement · Verdict 2956 · C 50
What advertising claims
What independent, higher-quality research supports
△ GAP
01

What the research actually shows

Multicenter double-blind placebo-controlled trial CT-OW-02 randomized 106 diagnosed premenopausal women with telogen effluvium, 53 per group, for six months. The primary endpoint was change in hair density by TrichoScan phototrichoscopy. NCT07111312 was first posted on August 8, 2025, after primary completion on May 10, 2024, so it cannot serve as prospective registration. Detailed missing-data handling and random-sequence and allocation-concealment methods were not confirmed in the public paper. The study did not collect minor adverse events at all. General tolerability therefore cannot be assessed.

02

Why this is classified as C (50)

Hair-density measurement favored the product, but a surrogate endpoint, one manufacturer-only trial, and a 106-person sample give C with 50 points.

Counterpoint. The numeric increase is real within this trial, but it does not establish visible fullness, durability, or benefit of other formulations.

Rejudgment record. Cross-check applied — Positive TrichoScan hair-density result in one 106-participant manufacturer trial with retrospective registration and a small sample

Scoring profile behind this grade
EndpointSSurrogate marker - laboratory or imaging measures
ReplicationR1Single confirmatory trial
IndependenceI0Evidence comes only from manufacturer studies
Effect sizeE+Meets the clinically important threshold

The scoring table and the verdict agree (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
Six-month increase in TrichoScan hair density with this finished productCThe day-180 change was +27.31 versus +18.23 hairs/cm².
Visibly fuller hair?The primary endpoint was not appearance.

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
Study 1Multicenter double-blind placebo-controlled randomized trial53Fully funded by Olistic Research Labs S.L., which supplied product and placebo and employed an authorIncrease in TrichoScan hair density at day 180+27.31±2.61 vs +18.23±2.98 hairs/cm², P<.01; 95% CI not reportedPivotal but retrospectively registered single manufacturer trial
§

Receipt — 1 References

All 1 cited sources were verified for existence at the original page (as of 2026-08-26).

Sáez Moya M, et al. Efficacy and Safety of a Drinkable Nutraceutical in Premenopausal Women with Telogen Effluvium. Dermatol Ther (Heidelb). 2025. PMID: 41288927.
checked
Research and draft: AI used · Cross-check: blind grading and adversarial audit
Final verification and publication gate: Codex · Verification cutoff: 2026-08-26 · Corrections: none

Cite this verdict

Benefit of Olistic Women for Hair Density in Telogen Effluvium Evidence Grade C card
[Chamgap] Benefit of Olistic Women for Hair Density in Telogen Effluvium — Evidence Grade C·50. 1 cited sources checked. Source: https://chamgap.com/en/verdicts/skin-hair/olistic-women-telogen-effluvium-hair-density/ · CC BY 4.0

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

!

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.