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NCT02470793 Clinical Trial

Technique And Results In Endothelial Keratoplasty

Fuchs' Endothelial Dystrophy Clinical Trial

— TREK  

Official title:
Technique And Results Evaluation In Endothelial Keratoplasty

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT02470793
Other study ID # 00001
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date September 2014
Est. completion date January 2021

Study information
Verified date March 2021
Source Hospital Mutua de Terrassa
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

To assess and compare the complications and results of different lamellar endothelial keratoplasty techniques and its variations.

Recruitment information / eligibility
Status Completed
Enrollment 62
Est. completion date January 2021
Est. primary completion date January 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: 1. Diagnosis with corneal endothelial dysfunction requiring lamellar endothelial corneal transplantation. 2. Free acceptance to be enrolled in the trial, and signature of the informed consent by the subject and/or its legal representatives. Exclusion Criteria: N/A

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• Descemet Stripping Automated Endothelial Keratoplasty
Descemet Stripping Automated Endothelial Keratoplasty
• Descemet Membrane Endothelial Keratoplasty
Descemet Membrane Endothelial Keratoplasty

Locations
Country Name City State
Spain Hospital Universitari Mutua Terrassa Terrassa Barcelona

Sponsors (1)
Lead Sponsor Collaborator
EDUARD PEDEMONTE-SARRIAS

Country where clinical trial is conducted

Spain, 

Outcome
Type Measure Description Time frame Safety issue
Primary Visual acuity First six months postoperatively
Secondary Endothelial cell density First six months postoperatively
Secondary Intraoperative complications First six months postoperatively
Secondary Postoperative complications First six months postoperatively
See also
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Completed NCT04420429 - The Effect Of Preoperative Parameters On Success After DMEK Surgery