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Prognosis of Posterior Lamellar Keratoplasty, an Observational Cohort Study (CORNEACOHORT)

C

Centre Hospitalier Régional Metz-Thionville

Status

Enrolling

Conditions

Pseudophakic Bullous Keratopathy
Fuchs' Endothelial Corneal Dystrophy

Treatments

Procedure: visual acuity comparaison

Study type

Observational

Funder types

Other

Identifiers

NCT06859411
2024-11Obs-CHRMT

Details and patient eligibility

About

Over the past decade, the management of Fuchs' endothelial corneal dystrophy (FECD) and pseudophakic bullous keratopathy (PBK) has been revolutionized by the development of posterior lamellar keratoplasty techniques: DSAEK and DMEK.

DSAEK (Descemet Stripping Automated Endothelial Keratoplasty) involves replacing the patient's endothelium and pathological descemetum with a descemetic endothelial graft combined with a thin stromal lamella. The endothelial density of the grafts is generally greater than 2,400 cells/mm². Depending on the grafting center and tissue bank, grafts may be either pre-cut in the tissue bank or cut on the operating table by the surgeon himself.

The donor graft is placed on an artificial anterior chamber, and automated microkeratome cutting produces grafts with an average thickness of 100 to 200µm, sometimes less than 100um (known as UT-DSAEK or ultra-thin DSAEK).

DMEK (Descemet Membrane Endothelial Keratoplasty) is a strictly endothelium and Descemet's membrane graft, as close as possible to the original anatomy of the cornea. The graft is dissected manually either in a tissue bank (pre-cut grafts) or on the operating table by the surgeon. The thickness of the graft is between 15 and 18 microns.

The primary objective of this observational cohort is to compare the evolution of visual acuity after DMEK, DSAEK or UT-DSAEK transplantation.

Secondary objectives are to compare the evolution of endothelial cell density, corneal thickness and early and late post-operative complications, and to identify factors predictive of these different endpoints.

Enrollment

1,000 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • patients who received a posterior lamellar keratoplasty in Metz-Thionville Regional Hospital between 2012 and 2030

Exclusion criteria

  • patients refusing to take part in the study

Trial design

1,000 participants in 3 patient groups

DMEK
Description:
Patients who received Descemet Membrane Endothelial Keratoplasty
Treatment:
Procedure: visual acuity comparaison
DSAEK
Description:
Patients who received Descemet Stripping Automated Endothelial Keratoplasty with preoperative graft thicker than 160 µm
Treatment:
Procedure: visual acuity comparaison
UT-DSAEK
Description:
DSAEK: patients who received Descemet Stripping Automated Endothelial Keratoplasty with preoperative graft thinner than 160 µm
Treatment:
Procedure: visual acuity comparaison

Trial contacts and locations

1

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Central trial contact

Arpiné EL NAR, PhD

Data sourced from clinicaltrials.gov

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