Spring Loaded Syringe for Active Silicon Oil Extraction
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Vitrectomy machine, Spring loaded syringe.
- Who it may be relevant to
- Registry conditions: Retinal Detachment. Basic parameters: from 18 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Egypt
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Official title
Vitrectomy Machine Versus Spring Loaded Syringe for Active Silicon Oil Extraxtion
Overview
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 for SOR into two groups:- Group A: SOR was performed using SO extraction program built in Optikon vitrectomy device Group B: SOR was performed using modified spring loaded syringe.
Interventions
- Device Vitrectomy machine
Active silicon oil extraction through 23G pars plana system vitrectomy machine - Device Spring loaded syringe
5 mml syringe with spring in its plunger and rubber connection
Primary outcome measures
- Incidence of complications [Time frame: During the surgical procedure and up to 3 months postoperative]
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
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Allocation
- Randomized
- Model
- Parallel assignment
- Masking
- Double blind
- Primary purpose
- Treatment
Study locations
Egypt · 1 center
- Sohag Faculty of Medicine — Sohag
Identifiers
NCT: NCT07363889 · Soh-Med-25-11-9PD