CHAMGAP
APPROVEDReviewed and approved by the Chamgap Editorial Team (2026-07-11). The draft was written by AI, the existence of all 2 cited sources was verified at the original page, and the verdict passed blind grading and adversarial audit. Methodology v0.6.
Verdict No. 304 · Search date 2026-07-11 · Methodology v0.6

Tisochrysis lutea powder,
does it really help with Improvement of dry-eye symptoms and tear secretion?

30-Second Summary
C
Evidence Grade C · 58 · Safety acceptable
T. lutea powder improved OSDI in one RCT, but objective tear-film results were partial
What the
research shows
In a randomized trial of 100 participants, OSDI decreased more with 900 mg/day for 12 weeks than with placebo, and some Schirmer-test results improved. The grade is C because only one Korean study exists and tear break-up time results were limited by time point and eye.
What the
ads claim
Advertisements may broadly claim tear generation and ocular-surface restoration. The clearest clinical result is a 12-week OSDI change in adults with mild symptoms; treatment of severe dry eye and long-term recurrence prevention were not evaluated.
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Useful facts when choosing a product

  • The clinical dose was 900 mg/day for 12 weeks.
  • Participants had OSDI scores of 13 to 32 and used digital devices for at least four hours daily.
  • Ninety-three participants completed the study.
  • The paper reported no major safety concern.
Gap Measurement · Verdict 304 · C 58
What advertising claims
What independent, higher-quality research supports
△ GAP
01

What the research actually shows

The 2024 study by Kim and colleagues randomized 100 adults with mild dry-eye symptoms who used digital devices for at least four hours daily to T. lutea powder at 900 mg/day or a maltodextrin placebo. Ninety-three completed the trial; at week 12, OSDI changed from 19.78 to 13.27 in the test group and from 21.35 to 18.48 in controls. Schirmer testing increased from baseline in both eyes in the test group, while significant tear break-up time findings were limited to the right eye at week six. The authors declared no conflicts, but no independent replication exists.

02

Why this is classified as C (58)

Regulatory recognition is not grading evidence. A positive primary OSDI endpoint and supportive tear-secretion signals favor human efficacy, but public evidence consists of one manufacturer-specific proprietary-product RCT, objective measures were only partly consistent, and independent replication is absent. This supports C with 58 points.

Counterpoint. A symptom-improvement signal was confirmed in adults with mild dry eye using the exact powder at 900 mg/day for 12 weeks.

Rejudgment record. Reassessment (cross-check reflected) — Regulatory recognition is not grading evidence; the primary 12-week OSDI endpoint and some Schirmer results were positive in one 100-person trial of a manufacturer-specific proprietary product, but tear break-up time and staining findings were limited and no independent replication exists

Cross-check — Codex and Claude

This verdict was drafted by Codex through literature review and source-existence checks, cross-checked through blind grading and adversarial audit, and settled by reapplying the methodology boundary rules. Cases with split grades were resolved through rejudgment.
03

Evidence Table

StudyDesignSampleFundingEndpointResultWeight
Kim CW et al. 2024Randomized placebo-controlled human trial12The paper declared no conflicts; detailed funding was unclearPrimary OSDI endpoint, Schirmer test, tear break-up time, and corneoconjunctival stainingA between-group difference in OSDI at week 12 and some Schirmer improvement; positive tear break-up time findings were limited by time point and eye.Key
Hong SC et al. 2022Cell and mouse mechanistic study7Supported by the Korean oceans ministry and KIST; a coauthor was affiliated with the ingredient companyTear volume, corneal damage, and inflammatory pathwaysImproved tear volume and tissue measures in a scopolamine dry-eye mouse model.Supportive
§

Receipt — 2 References

All 2 cited sources were verified for existence at the original page (as of 2026-07-11).

Kim CW, Kim H, Park YY, Park Y, Cho KJ. 2024. Effects of Tisochrysis lutea on Dry Eye Symptoms. Annals of Optometry and Contact Lens. 23(4):157-170. DOI: 10.52725/aocl.2024.23.4.157.
checked
Hong SC, Yu HS, Kim JW, Lee EH, Park CH, Hong KW, Kim JC. 2022. Protective effect of Tisochrysis lutea on dry eye syndrome via NF-κB inhibition. Scientific Reports. 12:19576. PMID: 36380046. DOI: 10.1038/s41598-022-23545-7.
checked
Draft and rewrite: Codex (AI) · Verification: Codex blind grading and adversarial audit · Final adjudication: Claude
Reviewed and approved: Chamgap Editorial Team · Approval date: 2026-07-11 · Corrections: none

Cite this verdict

Tisochrysis lutea powder × Improvement of dry-eye symptoms and tear secretion Evidence Grade C card
[Chamgap] Tisochrysis lutea powder × Improvement of dry-eye symptoms and tear secretion — Evidence Grade C·58. 2 cited sources checked. Source: https://health-receipt.pages.dev/en/verdicts/eye/tisochrysis-lutea-dry-eye/ · 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.