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OpenTrials
Completed

NCT Number: NCT03355924

DMEK And Cataract Surgery: Comparison Of Sequential Versus Combined Procedure

The aim of this study is to describe the outcomes of phaco-DMEK (Descemet Membrane Endothelial Keratoplasty ) according to a sequential versus a combined procedure

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Key information

Conditions

Cataract Corneal Graft Eye Diseases Lens Diseases

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

About this study

The study included patients who underwent DMEK combined or not with cataract surgery between January 2014 and march 2016. Were excluded patients with other ocular comorbidity, and those who had graft after a first graft failure. The main outcome was BVCA measured at one year. The post-operative follow up was down at D7, M1, M3, M6, and M12. Secondary outcomes were; the mean time to visual recovery and influence of the delay between cataract removal and DMEK.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • patients who underwent DMEK combined or not with cataract surgery

Exclusion criteria

  • patients with other ocular comorbidity, and those who had graft after a first graft failure

Treatment and study plan

Primary outcomes

  1. Best visual acuity

    Time frame: Month 12

    logMar

Sponsors and collaborators

Lead sponsor

Centre Hospitalier Régional Metz-Thionville

Other

Registry information

Acronym: CISIPHE

Important dates

Study start
2016
Primary completion
2017
Study completion
2017
First posted
Nov 28, 2017
Registry last updated
Aug 24, 2023

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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