Last reviewed · How we verify
NCT05892185
Evaluate the Efficacy and Safety of Glaucoma Implant in Primary Open Angle Glaucoma
NA trial testing GELA in Glaucoma in 20 participants. Status unknown.
12 January 2024
Quick facts
| Lead sponsor | Mingche Biotechnology CO., LTD |
|---|---|
| Phase | NA |
| Status | Status unknown |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | single |
| Primary purpose | treatment |
| Enrollment | 20 |
| Start date | 31 May 2023 |
| Primary completion | 12 January 2024 |
| Estimated completion | 19 July 2024 |
Drugs / interventions tested
- GELA
- XEN
Conditions studied
- Glaucoma — all drugs for Glaucoma →
Sponsor
Mingche Biotechnology CO., LTD
Who can join
Adults 18 to 75, any sex, with Glaucoma. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
The objective of this study is to evaluate the efficacy and safety of glaucoma device in the treatment of primary open-angle glaucoma.
Publications & conference data
No peer-reviewed publications indexed yet for this trial.
Verify or expand the search:
- PubMed search for NCT05892185
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
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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 NCT05892185 (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 Mingche Biotechnology CO., LTD
- Last refreshed: 7 June 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/NCT05892185.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing