Endothelial Corneal Dystrophy Clinical Trial
— GOODRMEKOfficial title:
Predictive Factors of Good Results After Primary Descemet's Membrane Endothelial Keratoplasty (DMEK): Retrospective Study About 102 Eyes
NCT number | NCT04469933 |
Other study ID # | 2020-03ObsCHRMT |
Secondary ID | |
Status | Completed |
Phase | |
First received | |
Last updated | |
Start date | May 1, 2016 |
Est. completion date | May 1, 2018 |
Verified date | June 2020 |
Source | Centre Hospitalier Régional Metz-Thionville |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
Aim: Identify predictive factors of good results after primary Descemet's Membrane
Endothelial Keratoplasty (DMEK) in Fuchs Endothelial Corneal Dystrophy (FECD).
82 patients (102 eyes) with Fuchs Endothelial Corneal Dystrophy (FECD) underwent DMEK between
March 2016 and March 2018 were analyzed. Follow-up time was 12 months. The studied prognostic
criteria were: pre-operative Central Corneal Thickness (CCT), CCT's delta between pre and D15
post-operatively, anterior mean keratometry, pre-operative endothelial cell density (ECD) and
postoperative ECD at 6 and 12 months, pre-operative visual acuity, donors' and recipients'
ages, recipients' sex, rebubbling and triple procedure (DMEK combined with cataract surgery).
Status | Completed |
Enrollment | 102 |
Est. completion date | May 1, 2018 |
Est. primary completion date | May 1, 2018 |
Accepts healthy volunteers | |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - Over 18, - had advanced FECD associated with visual symptoms and reduced visual acuity . Exclusion Criteria: - Prior intraocular surgery other than cataract - Other indications for DMEK surgeries than FECD, - Eyes with corneal (except FECD), retinal or optic nerve diseases - Per-operative difficulties (tear's graft or complicated unfolding graft) - Primary graft failure (cornea that failed to clear in the presence of an attached graft) - Secondary graft failure (corneal decompensation after an initial period of a functional graft) |
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
Centre Hospitalier Régional Metz-Thionville |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Pre-operative Central Corneal Thickness (CCT), | Pre-operative CCT (µm) measured by an anterior segment optical coherence tomography (AS-OCT; RS-3000; Nidek Co. Ltd, Japan) | day 1 | |
Primary | Post-operative Central Corneal Thickness (CCT), | Post-operative CCT (µm) measured by an anterior segment optical coherence tomography (AS-OCT; RS-3000; Nidek Co. Ltd, Japan) | Months 12 | |
Primary | CCT's delta | CCT's delta (µm) between pre and D15 post-operatively | day 15 | |
Secondary | anterior mean keratometry | anterior mean keratometry (calculated by an auto keratometer Visionix Luneau L67, France) | day 1 | |
Secondary | pre-operative endothelial cell density ECD | pre-operative ECD (using a non-contact specular microscope CEM-530; Nidek Co. Ltd, Japan) | day1 | |
Secondary | post-operative endothelial cell density (ECD) | post-operative ECD at 6 months (using a non-contact specular microscope CEM-530; Nidek Co. Ltd, Japan) | 6 months | |
Secondary | post-operative endothelial cell density (ECD) | post-operative ECD at 12 months (using a non-contact specular microscope CEM-530; Nidek Co. Ltd, Japan) | 12 months | |
Secondary | pre-operative Visual Acuity | pre-operative Visual Acuity (using Monoyer chart and converted it to logMar scale) | day 1 | |
Secondary | donors' and recipients' ages | donors' and recipients' ages | day 1 | |
Secondary | recipients' sex | recipients' sex | day 1 | |
Secondary | rate of rebubbling | the rate of rebubbling %(postoperative graft detachment) | months 6 |
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