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NCT05601011
Changes of Clinical Characteristics and Tear Film Biomarkers Following FS-LASIK
trial in Dry Eye in 60 participants. Status unknown.
19 October 2023
Quick facts
| Lead sponsor | Peking University Third Hospital |
|---|---|
| Status | Status unknown |
| Study type | OBSERVATIONAL |
| Enrollment | 60 |
| Start date | 31 October 2022 |
| Primary completion | 19 October 2023 |
| Estimated completion | 19 October 2023 |
| Sites | 1 location across China |
Conditions studied
- Dry Eye — all drugs for Dry Eye →
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:
- PubMed search for NCT05601011
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
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Other Peking University Third Hospital trials
Trials by the same sponsor.
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Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT05601011 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Peking University Third Hospital
- Last refreshed: 13 September 2023
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