Spring Loaded Syringe for Active Silicon Oil Extraction

Recruiting N/A Interventional Study
Retinal Detachment
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 and older
Sex
Any
Study type
Interventional
Purpose
Treatment
Participants needed
200 (estimated)
Sponsor
Sohag University · Other
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About This Trial
The aim of our study is to compare between two techniques used for active SOR. The outcomes include efficiency and safety. Patients with silicon filled eyes and prepared for SOR 540 eyes of 505 patients (one eye in 470 patients, and both eyes in 35 patients) were enrolled in the study. All eyes underwent SOR using 23-Gauge PPV. The eyes were classified according to the surgical technique used fo…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Patients subjected previously to pars plana vitrectomy with silicon oil tamponade. Exclusion Criteria: * Recurrent retinal detachment * Previous scleral buckling * Previous glaucoma surgery * Bleeding tendencies * Anterior staphyloma
Contacts

Alaa A A Sinjab, Doctor degree in Ophthalmology

+20-01064037382

alaa.abdelsadek@med.sohag.edu.eg

CONTACT