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OpenTrials
Completed

NCT Number: NCT03685851

Post Operative Visual Acuity for DSAEK and UT-DSAEK

To study the correlation between graft size in DSAEK (Descemet Stripping Automated Endothelial Keratoplasty) and UT (ultra thin)-DSAEK type corneal transplants to the visual acuity 6 months postoperatively.

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Key information

Conditions

Corneal Transplant

Sex eligibility

All sexes

Study type

Observational

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Patients who underwent DSAEK surgery
  • Patients in department of ophthalmology between february 2012 and june 2017

Exclusion criteria

  • None

Treatment and study plan

DSAEK type corneal transplant

Procedure

All surgeries were performed by the same surgeon and according to the same protocol

Primary outcomes

  1. Postoperative visual acuity

    Time frame: Month 6

    postoperative visual acuity in logmar

Secondary outcomes

  1. Pachymetry

    Time frame: Month 6

    Measurement of the thickness of the cornea

Sponsors and collaborators

Lead sponsor

Centre Hospitalier Régional Metz-Thionville

Other

Registry information

Official study title

Post Operative Visual Acuity for Descemet Stripping Automated Endothelial Keratoplasty (DSAEK) and UT-DSAEK

Acronym: POVIAD

Important dates

Study start
2012
Primary completion
2015
Study completion
2017
First posted
Sep 26, 2018
Registry last updated
Oct 11, 2018

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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