ClinicalTrials.Veeva

Menu

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

D

Dar El Oyoun Hospital

Status

Completed

Conditions

Retinal Detachment

Treatments

Other: Silicone oil Tamponade for Retinal Detachment

Study type

Observational

Funder types

Other

Identifiers

NCT05817630
N-19-2023

Details and patient eligibility

About

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

Full 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

Enrollment

32 patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion criteria

  • • Silicone oil (SO) tamponade ( up to 6 months)

    • Attached retina under SO
    • Attached retina 3 months after Silicone oil Removal (SOR)
    • Normal fellow eye ( no retinal detachment or macular disease)
    • OCT scan performed for the operated eyes (before SOR, and 3 months after SOR), and for the fellow eye (at any time during the study)

Exclusion criteria

  • • Rhegmatogenous Retinal Detachment (RRD) with other tamponades ( e.g.: Gas, Densiron)

    • SO tamponade less than 3 months, or more than 6 months
    • Recurrent RD under SO
    • Recurrent RD within 3 months after SOR
    • One eyed
    • Vitrectomized fellow eye
    • Retinal detachment, or macular disease in the fellow eye.
    • Posterior staphyloma
    • Anisometropia (history, refraction if possible, spectacles prescription)
    • Absence of any of the OCT scans performed for the operated eyes (before SOR, and 3 months after SOR), and for the fellow eye (at any time during the study)

Trial design

32 participants in 2 patient groups

Group A
Description:
Group A: 3 months SO Tamponade
Treatment:
Other: Silicone oil Tamponade for Retinal Detachment
Group B
Description:
Group B: 6 months SO Tamponade
Treatment:
Other: Silicone oil Tamponade for Retinal Detachment

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems