Skip to content

DMEK Endothelial Keratoplasty in Patients With a History of Anterior or Posterior Segment Surgery

DMEK Endothelial Keratoplasty in Patients With a History of Anterior or Posterior Segment Surgery : Serious Complication Rate and Visual Efficacy at 12 Months

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06013462
Acronym
DMEK complexes
Enrollment
80
Registered
2023-08-28
Start date
2024-03-15
Completion date
2028-04-30
Last updated
2025-12-08

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

Conditions

Patients Undergoing DMEK With a History of Anterior or Posterior Segment Surgery

Brief summary

DMEK (Descemet Membrane Endothelial Keratoplasty) is a surgical technique used to treat primary or secondary corneal endothelial decompensation. At the Rothschild Foundation, as in many Western referral centers, DMEK is currently the surgical technique of choice for the treatment of primary or secondary corneal endothelial decompensation. Technically challenging, it is a relatively tedious surgery to learn, but offers the best visual and refractive results, as well as faster visual and functional recovery in simple cases. In patients without anterior or posterior segment surgical history, the complication rate of DMEK, including graft rejection, is similar to that of other endothelial keratoplasty surgical techniques. However, in specific cases, in patients with a history of ophthalmological surgery such as vitrectomy, trabeculectomy, large iris defects, anterior synechiae, aniridia or aphakia, the scientific literature shows a higher complication rate for DMEK (increased rate of rebulling and graft decompensation). As a result, other techniques that are less effective on visual results continue to be used for these patients in a large number of centers. Nonetheless, in our department, DMEK is also performed on these complicated patients. When it comes to patients with a history of anterior or posterior segment surgery, it seems to us that the surgeons' experience with DMEK allows better visual results than with any other technique, but without any back up regarding the complication rate in the literature. The main aim of this study is to describe, in patients with a history of anterior or posterior segment surgery undergoing DMEK, the 12-months occurrence rate of at least one serious post-operative complication.

Interventions

DMEK (Descemet Membrane Endothelial Keratoplasty) is a surgical technique used to treat primary or secondary corneal endothelial decompensation.

Sponsors

Fondation Ophtalmologique Adolphe de Rothschild
Lead SponsorNETWORK

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

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

Inclusion criteria

: * Patients scheduled for corneal endothelial transplantation in one or both eyes * History of vitrectomy, trabeculectomy, large iris defects, anterior synechiae on the eye to be operated on * Pseudophakia or aphakia in the eye to be operated on * Express consent to participate in the study * Affiliated or beneficiary of a social security scheme

Exclusion criteria

: * Need for combined PKE + EK surgery * Primary endothelial decompensation * At least one contraindication to endothelial transplantation : * Presence of a stromal corneal cleft * Inflammatory or degenerative corneal pathology other than endothelial * Progressive corneal infection * Degenerative retinal pathology not allowing visual recovery postoperatively (for the purposes of this study, we accept patients who have had retinal detachment and whose loss of vision is clearly attributable to endothelial decompensation) * End-stage glaucoma not allowing visual recovery post-operatively (for this study, we accept patients who have had filtering surgery for glaucoma, which is stabilized at the time of surgery. Decline in vision must be clearly attributable to endothelial decompensation) * Medical contraindication to general or local anesthesia * Patient under legal protection * Pregnant or breast-feeding women

Design outcomes

Primary

MeasureTime frameDescription
Occurrence rate of at least one serious DMEK post-op complication12 monthsComposite endpoint made of 4 serious post-op complications : * Rebulling : graft detachment of more than one-third of its surface area one week after surgery (on Avanti OCT-cornea), requiring air or gas injection in the anterior chamber. * Graft failure : no improvement in pachymetry at three months post-op (Avanti OCT-cornea). * Graft rejection : presence of cellular Tyndall in the anterior chamber and/or retro-descemetic precipitates and/or focal or diffuse increase in pachymetry \> 20μm (Avanti OCT-cornea and slit-lamp biomicroscopic examination). * Macular cystoid edema : presence of intraretinal fluid in the macular area (macular OCT).

Secondary

MeasureTime frameDescription
Graft failure occurrence rate12 monthsNo improvement in pachymetry at three months post-op (Avanti OCT-cornea).
Graft rejection occurrence rate12 monthsPresence of cellular Tyndall in the anterior chamber and/or retro-descemetic precipitates and/or focal or diffuse increase in pachymetry \> 20μm (Avanti OCT-cornea and slit-lamp biomicroscopic examination).
Macular cystoid edema occurrence rate12 monthsPresence of intraretinal fluid in the macular area (macular OCT).
Intraocular hypertension occurrence rate12 monthsIntraocular pressure greater than 21mmHg measured by pneumotonometer or applanation tonometer.
Graft detachment (with or without rebulling) occurrence rate12 monthsFailure of the graft to press against the posterior host corneal stroma (Avanti OCT-cornea and slit-lamp biomicroscopic examination).
Surgeon's subjective assessment of surgical complexityRight after the completion of the surgeryEvaluation by the main surgeon at the end of the procedure, on a Likert scale from 0 to 10 (0 being normal, uncomplicated surgery and 10 being the maximum level of complexity encountered).
Rebulling occurrence rate12 monthsGraft detachment of more than one-third of its surface area one week after surgery (on Avanti OCT-cornea), requiring air or gas injection in the anterior chamber.
Evolution of visual results (corrected and uncorrected)1 month after surgeryMeasurements with optotypes : Best monocular visual acuity (decimal scale converted to logMAR)
Evolution of refractive results1 month after surgeryNidek® autorefractometer measurement : 1. Sphere (in dioptres) 2. Cylinder (in dioptres) 3. Spherical equivalent (in dioptres) 4. Cylinder axis (in degrees)
Evolution of endothelial loss1 month after surgeryMeasurement by central and peripheral specular microscopy (4 measurements performed nasally, temporally, superiorly and inferiorly). Endothelial loss in each quadrant is defined as a decrease in endothelial count (cells/mm²) expressed as a % relative to the pre-operative measurement.
Evolution of corneal thickness1 month after surgeryCorneal thickness in μm measured by OCT - Avanti® type cornea.
Evolution of posterior keratometry1 month after surgeryPosterior keratometry in diopters measured by Scheimpflug corneal topography (Pentacam®).
Duration of surgical procedure (in minutes)Right after the completion of the surgeryThe start of the procedure is defined by the placement of the blepharostat and the end of the procedure is defined by the end of the lens dressing.

Countries

France

Contacts

Primary ContactAmélie YAVCHITZ
ayavchitz@for.paris01.48.03.64.33

Outcome results

None listed

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