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NCT04424550: DEMOGRAFT

Comparative Results After DSAEK, UT-DSAEK and DMEK for Fuchs Endothelial Corneal Dystophy

Completed Last updated 11 June 2020
What this trial tests

trial in Corneal Dystrophy in 218 participants. Completed in 1 August 2019.

Timeline
1 August 2017
Primary endpoint
1 August 2019
1 August 2019

Quick facts

Lead sponsorCentre Hospitalier Régional Metz-Thionville
StatusCompleted
Study typeOBSERVATIONAL
Enrollment218
Start date1 August 2017
Primary completion1 August 2019
Estimated completion1 August 2019
Sites1 location across France

Conditions studied

Sponsor

Centre Hospitalier Régional Metz-Thionville

Who can join

18 and older, any sex, with Corneal Dystrophy. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Purpose of the research is to describe and compare the evolution of BSCVA after DMEK, DSAEK and UT-DSAEK for Fuchs Endothelial Corneal Dystrophy (FECD) and Moderate Pseudophakic Bullous Keratopathy (PBK). To secondarily research the correlates criterions with best spectacle corrected visual acuity (BSCVA) 12 months postoperatively.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other recruiting trials for Corneal Dystrophy

Currently open trials in the same condition.

Other Centre Hospitalier Régional Metz-Thionville 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/NCT04424550.

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