Clinical Trials Directory

Trials / Not Yet Recruiting

Not Yet RecruitingNCT06240364

Effects of AffronEye®/ Crocuvis+® on Dry Eye Syndrome

Status
Not Yet Recruiting
Phase
N/A
Study type
Interventional
Enrollment
204 (estimated)
Sponsor
University of Alicante · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Previous research has demonstrated the effectiveness of AFFRONEYE® / CROCUVIS+® dietary supplement, based on saffron extract, in the proper functioning of visual health, for example, against the development of glaucoma. The main objective of this study is to compare the results of clinical tests that evaluate signs and symptoms for the diagnosis of dry eye, between two groups (some that take the dietary supplement and others a placebo), in a sample of university workers and students who suffer from dry eye.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTSaffron extract (Crocus sativus)Daily intake of one tablet for 84 days.
DIETARY_SUPPLEMENTPlaceboDaily intake of one tablet for 84 days.

Timeline

Start date
2025-10-10
Primary completion
2026-04-30
Completion
2026-12-30
First posted
2024-02-05
Last updated
2025-04-01

Locations

1 site across 1 country: Spain

Source: ClinicalTrials.gov record NCT06240364. Inclusion in this directory is not an endorsement.