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OpenTrials
Completed

NCT Number: NCT02470793

Technique And Results In Endothelial Keratoplasty

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

Completed

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Key information

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Diagnosis with corneal endothelial dysfunction requiring lamellar endothelial corneal transplantation.
  • 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

Treatment and study plan

Descemet Stripping Automated Endothelial Keratoplasty

Procedure

Descemet Stripping Automated Endothelial Keratoplasty

Other names: DSAEK, DSEK

Descemet Membrane Endothelial Keratoplasty

Procedure

Descemet Membrane Endothelial Keratoplasty

Other names: DMEK

Primary outcomes

  1. Visual acuity

    Time frame: First six months postoperatively

Secondary outcomes

  1. Endothelial cell density

    Time frame: First six months postoperatively

  2. Intraoperative complications

    Time frame: First six months postoperatively

  3. Postoperative complications

    Time frame: First six months postoperatively

Sponsors and collaborators

Lead sponsor

EDUARD PEDEMONTE-SARRIAS

Other

Registry information

Official study title

Technique And Results Evaluation In Endothelial Keratoplasty

Acronym: TREK

Important dates

Study start
2014
Primary completion
2021
Study completion
2021
First posted
Jun 12, 2015
Registry last updated
Mar 11, 2021

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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