Clinical Trials in Egypt / NCT07418606
Active, not recruiting
Observational
Corneal Endothelial Cell Changes In Silicon Filled Eye
NCT07418606 · tracked via the Priya Life Science Egypt tracker
Condition(s) studied
Rhegmatogenous Macula-off Retinal Detachment
Study summary
The aim of this study is to evaluate corneal endothelial cell changes after pars plana vitrectomy in Rhegmatogenous Retinal detachment , compare the results using different silicon oil viscositites , and assess whether these changes are reversible after silicone removal or not .
Eligibility
Inclusion Criteria:
\- All patients with Rhegmatodenous retinal detachment which need PPV will be included in this study.
Exclusion Criteria:
* Patients with corneal dystrophies or degeneration.
* Patients with a history of refractive surgery, either corneal or phakic lOL implantation.
* Patients with a history of keratoplasty.
* Patients with history of retinal detachment surgery in the same eye.
* Recurrent cases during the follow-up period will be removed from the study. 6. patients with gas tamponade 7. patients with silicon oil 1000 cs 8. patients with Retinal pathologies such as macular hole , diabetic changes 9. patients undergo phacovitrectomy
Primary outcome measure(s)
- Corneal Endothelial Cell Changes In Silicon Filled Eye . — 4 months
Corneal Endothelial Cell Changes cell density ( cells/ mm) , coeffient variation(%) In Silicon Filled Eye at 1 and 3 months postoperative
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| Minia University | Minya | Egypt |
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Official registry record
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT07418606 on ClinicalTrials.gov ↗ ← All trials in Egypt