Clinical Trials Directory

Trials / Completed

CompletedNCT05817630

Duration of Silicone Oil Tamponade on Foveal and Parafoveal Thickness in Rhegmatogenous Retinal Detachment

Impact of Duration of Silicone Oil Tamponade on Foveal and Parafoveal Thickness in Rhegmatogenous Retinal Detachment: A Retrospective Cohort Study

Status
Completed
Phase
Study type
Observational
Enrollment
32 (actual)
Sponsor
Dar El Oyoun Hospital · Academic / Other
Sex
All
Age
Healthy volunteers
Not accepted

Summary

Our study observes and analyses the influence of the duration of tamponade with silicone oil on the foveal and parafoveal thickness.

Detailed description

Retrospective Cohort study Retrospective review of records of eyes with Rhegmatogenous Retinal Detachment (RRD, for whom pars plana vitrectomy and silicone oil had been performed, in the period between January 2019 and December 2021. After checking inclusion and exclusion criteria; we will enroll all the cases. We shall observe the duration of silicone oil tamponade, and then divide the cases; accordingly; into 2 groups (Cohort). * Group A: 3 months SO Tamponade * Group B: 6 months SO Tamponade

Conditions

Interventions

TypeNameDescription
OTHERSilicone oil Tamponade for Retinal Detachmenteyes with Rhegmatogenous Retinal Detachment (RRD, for whom pars plana vitrectomy and silicone oil had been performed

Timeline

Start date
2023-02-15
Primary completion
2023-04-01
Completion
2023-04-05
First posted
2023-04-18
Last updated
2023-04-18

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT05817630. Inclusion in this directory is not an endorsement.