Preoperative Corneal Thickness and Postoperative Visual Outcomes After Posterior Lamellar Corneal Transplant
NCT ID: NCT03355911
Last Updated: 2017-12-05
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
113 participants
OBSERVATIONAL
2016-10-01
2017-05-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
RETROSPECTIVE
Eligibility Criteria
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Inclusion Criteria
* Fuchs dystrophy,
* pseudophakic bullous decompensation
* or other endothelial dysfunction corneal
Exclusion Criteria
* the technical inability of preoperative CCT measurement
* the need for a penetrating keratoplasty following endothelial graft failure
* severe postoperative complications resulting in unquantifiable visual acuity
No
Sponsors
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Centre Hospitalier Régional Metz-Thionville
OTHER
Responsible Party
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Other Identifiers
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2016-07Obs-CHRMT
Identifier Type: -
Identifier Source: org_study_id