Clinical Characteristics and Surgical Outcomes of the Fellow Eye in Bilateral Retinal Detachments

Status

Not yet recruiting

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT06292572

Enrollment

Registered

2024-03-05

Start date

2024-03-01

Completion date

2024-11-01

Last updated

2024-03-05

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

Conditions

Retinal Detachment

Keywords

retinal detachment, bilateral, vitrectomy

Brief summary

To assess the clinical features and the surgical outcomes of RD repair surgery of the fellow eye in bilateral retinal detachments

Detailed description

Bilateral retinal detachment is a rare but sight-threatening disease, that can cause blindness and poor quality of life. It has been proved that patients who suffer from RD in one eye have a considerably increased risk to subsequently develop an RD in the fellow eye. It can be expected that patients who experienced a RD in one eye, tend to present sooner when experiencing a RD in the fellow eye, and thus have a greater visual and/or anatomical prognosis. In this study, we aim to describe characteristics of bilateral RD and compare the initial and subsequent eye in terms of clinical preoperative features, surgical management, and anatomical and visual results.

Interventions

PROCEDURERetinal Detachment Surgery

Retinal Detachment Surgery that consists in either Pars Plana Vitrectomy or Scleral Buckling or a combination of both techniques, and with or without use of intraocular tamponade

Study design

Observational model

COHORT

Time perspective

RETROSPECTIVE

Eligibility

Sex/Gender

ALL

Age

18 Years to No maximum

Healthy volunteers

Inclusion criteria

* All patients that underwent retinal detachment repair surgery for bilateral sequential retinal detachment between January 2016 and December 2023 at the Nancy Regional and University Hospital Center (via pars plana vitrectomy or scleral buckling) and with a minimum of 6 month of post-operative follow-up after the last surgery.

Exclusion criteria

* Patients that underwent surgery at another facility * Patients with a history of previous vitrectomy or * Patients with a history of trauma from a penetrating injury or ruptured globe, retinal neovascular condition, hereditary vitreo-retinopathy

Design outcomes

Primary

Measure	Time frame	Description
Rate of surgical success	6 month after surgery	Rate of succesful surgical repair of RD within the follow-up period

Secondary

Measure	Time frame	Description
Visual Acuity	6 month after surgery	LogMAR Visual acuity measured at the follow-up visit

Countries

France

Contacts

Primary ContactIda Gordon

gordon.ida14@gmail.com+33622820203

Backup ContactJean-Baptiste Conart, MD, PhD

jbconart@gmail.com

Outcome results

None listed

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