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Pratical Assessment of DSAEK in the Management of Endothelial Decompensation Following Penetrating Keratoplasty

Pratical Assessment of Descemet'Sstripping Automated Endothelial Keratoplasty (DSAEK) in the Management of Endothelial Decompensation Following Penetrating Keratoplasty

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03687996
Acronym
MADE
Enrollment
6
Registered
2018-09-27
Start date
2015-01-01
Completion date
2016-07-31
Last updated
2023-02-03

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

Conditions

Descemet's Stripping Automated Endothelial Keratoplasty

Brief summary

Reporting our anatomical and functional results and the possible complications of the first six Descemet's stripping endothelial keratoplasty (DSAEK) performed in our department secondary to endothelial decompensation after penetrating keratoplasty.

Detailed description

A retrospective and observational monocentric study fo six patients with DSAEK after prior penetrating keratoplasty (PK). The data collected are: demographic characteristics, ophthalmological comorbidities, initial indication of PK, delay between PK and DSAEK. Preoperative Visual Acuity and at 1, 3 and 6 months postoperative were collected in logmar for analysis. The central cornea and graft thickness measured in OCT as well as the postoperative complications were also collected.

Interventions

None listed

Sponsors

Centre Hospitalier Régional Metz-Thionville
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
RETROSPECTIVE

Eligibility

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

Inclusion criteria

* with endothelial decompensation after penetrating keratoplasty * surgery realised by the same surgeon

Exclusion criteria

* None

Design outcomes

Primary

MeasureTime frameDescription
visual acuitychange from visual acuity at 6 monthpre and postoperative visual acuity in logmar

Secondary

MeasureTime frameDescription
cornea thickness at 6 monthschange from cornea thickness at 6 monthsthe central cornea and graft thickness measured in OCT
cornea thickness at 10 yearschange from cornea thickness at 10 yearsthe central cornea and graft thickness measured in OCT
postoperative complicationsmonth 6all the postoperative complications were collected
visual acuity at 10 yearschange from visual acuity at 10 yearspre and postoperative visual acuity in logmar

Outcome results

None listed

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