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NCT05601011

Changes of Clinical Characteristics and Tear Film Biomarkers Following FS-LASIK

Status unknown Last updated 13 September 2023
What this trial tests

trial in Dry Eye in 60 participants. Status unknown.

Timeline
31 October 2022
Primary endpoint
19 October 2023
19 October 2023

Quick facts

Lead sponsorPeking University Third Hospital
StatusStatus unknown
Study typeOBSERVATIONAL
Enrollment60
Start date31 October 2022
Primary completion19 October 2023
Estimated completion19 October 2023
Sites1 location across China

Conditions studied

Sponsor

Peking University Third Hospital

Who can join

Adults 18 to 45, any sex, with Dry Eye. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

to analyze the clinical and tear molecular profile up to 6 months after FS-LASIK surgery

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

Verify or expand the search:

Other recruiting trials for Dry Eye

Currently open trials in the same condition.

Other Peking University Third Hospital trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05601011.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing