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Visual Outcomes Following Descemet Stripping Automated Endothelial Keratoplasty

Visual Outcomes Following Descemet Stripping Automated Endothelial Keratoplasty for Corneal Endothelial Dysfunction

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03685734
Acronym
VO-DSAEK
Enrollment
36
Registered
2018-09-26
Start date
2015-01-01
Completion date
2016-01-01
Last updated
2018-09-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Corneal Endothelial Disorder

Keywords

DSAEK

Brief summary

To assess objective and subjective visual outcomes achieved by patients with corneal endothelial dysfunction who have undergone surgical treatment with Descemet stripping automated endothelial keratoplasty (DSAEK).

Detailed description

Since 2006, the technique by removing the Descemet membrane from the recipient cornea was renamed Descemet stripping automated endothelial keratoplasty (DSAEK). In recent years, DSAEK techniques have evolved, favoring increasingly thinner and finer grafts, known as ultrathin DSAEK (UT DSAEK), with the aim of obtaining better visual results. Endothelial keratoplasty is now the most common surgical procedure used to treat endothelial dysfunction. The current study focused on assessing both objective and subjective visual quality outcomes following DSAEK.

Interventions

None listed

Sponsors

Centre Hospitalier Régional Metz-Thionville
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Clinical eligibility for DSAEK * Informed written consent * Successful completion of DSAEK procedure * Postoperative follow-up at least 1 year * Ability to respond to the questionnaire

Exclusion criteria

* Patients with clinical edematous cornea * With significant stromal opacity * With major disturbances of ocular surface * Previous corneal surgery

Design outcomes

Primary

MeasureTime frameDescription
Visual acuity1 yearScored with reference to the logarithm of the minimum angle of resolution (logMAR) and its variation in line gain.

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026