Clinical Trials in Taiwan / NCT06848829
Recruiting
Not applicable
Difference of Tear Ferning Between Women with and Without Menopausal.
NCT06848829 · tracked via the Priya Life Science Taiwan tracker
Condition(s) studied
Dry Eye Syndromes
Investigational drug(s) / intervention(s)
Pre-manepausal women
Pre-manepausal women: Compare tear ferning structure between pre-menopause and post-menopause women.
Study summary
Application of tear ferning test for clinical dry eye diagnosis and menopause
Eligibility
Inclusion Criteria:
* Aged between 20 and 65 years
Exclusion Criteria:
* No evident ocular diseases such as cornea, cataracts, vitreous degeneration, glaucoma, and retinopathy.
* Belong to vulnerable groups(pregnancy woman, prisoner, ethical minorities, economic or educationally disadvantaged subjects, disabled individuals such as those at terminal stage of tumorigenesis, blindness, terminal ill individuals)
Primary outcome measure(s)
- Schirmer's test — 5 minutes
To assess tear secretion volume - Tear film breakup time — 20 seconds
To assess tear quality - Ocular surface status — 3 minutes
To assess ocular surface health status with lissamine green stain, health or corneal abrasion. - Tear ferning — 30 minutes
crystal structure formed from tear drops on a slide be scored. - Menopause related hormone Enzyme-linked immunosorbent assay (ELISA) — 3 hours
To assess FSH/LH/E2/Progesterone/Mc5AC/Lactoferrin concentration between pre- and post-manopause women.
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| Jen-Ai Hospital | Taichung | Taiwan | Recruiting |
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Official registry record
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT06848829 on ClinicalTrials.gov ↗ ← All trials in Taiwan