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Spring Loaded Syringe for Active Silicon Oil Extraction

Vitrectomy Machine Versus Spring Loaded Syringe for Active Silicon Oil Extraxtion

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07363889
Enrollment
200
Registered
2026-01-23
Start date
2022-01-04
Completion date
2027-05-01
Last updated
2026-01-23

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

Conditions

Retinal Detachment

Keywords

Pars plana vitrectomy, Silicon oil tamponade, Silicon oil extraction

Brief summary

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

Active silicon oil extraction through 23G pars plana system vitrectomy machine

DEVICESpring loaded syringe

5 mml syringe with spring in its plunger and rubber connection

Sponsors

Sohag University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

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

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

Design outcomes

Primary

MeasureTime frameDescription
Incidence of complicationsDuring the surgical procedure and up to 3 months postoperativeIncidence of operative and postoperative complications in both groups

Countries

Egypt

Contacts

CONTACTAlaa A A Sinjab, Doctor degree in Ophthalmology
alaa.abdelsadek@med.sohag.edu.eg+20-01064037382

Outcome results

None listed

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