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REtinal Detachment Outcomes Study

Not Applicable
Recruiting
Conditions
Retinal Detachment
Interventions
Procedure: Pars plana vitrectomy
Procedure: Pars plana vitrectomy with scleral buckle
Other: Sulfur hexafluoride gas tamponade
Other: Perfluoropropane gas
Registration Number
NCT05863312
Lead Sponsor
CHU de Quebec-Universite Laval
Brief Summary

Background: Few large randomized controlled trials provide strong evidence to guide surgical repair of primary rhegmatogenous retinal detachment (RRD) repair. The purpose of this factorial, single-blind, randomized controlled trial is to analyze and compare the surgical outcomes, functional visual outcomes, complications, and quality of life associated with RRD repair using (A) pars plana vitrectomy only (PPV) or PPV with scleral buckle (PPV-SB) and (B) sulfur hexafluoride gas (SF6) or perfluoropropane gas (C3F8) tamponade.

Methods: Eligible patients with moderately complex RRD will be randomized 1:1 to PPV or PPV-SB and 1:1 to SF6 or C3F8 gas tamponade. Approximately 560 patients will be recruited to be able to detect a difference of around 10% in SSAS rate between groups. Patients will be followed using multimodal imaging and quality of life questionnaires before and after the surgical repair until 1 year postoperative. The primary outcome will be single surgery anatomic success (SSAS), defined as absence of reoperation for recurrent RRD in the operating room. Secondary outcomes will be pinhole visual acuity (PHVA) at 8-10 weeks and 6 months, final best-corrected visual acuity (BCVA), final retina status (i.e., attached or detached), time to onset of RRD recurrence, severity and number of complications, and questionnaire results.

Discussion: This will be the first 2 × 2 factorial randomized controlled trial examining repair techniques in primary RRD. It will also be the first randomized controlled trial to compare gas tamponade between the two most common agents. Notably, it will be adequately powered to detect a clinically significant effect size. The use of multimodal imaging will also be a novel aspect of this study, allowing us to compare head-to-head the impact of adding an SB to the retina's recovery after RRD repair and of differing gas tamponades. Until now, the treatment of RRD has been largely guided by pragmatic retrospective cohort studies. There is a lack of strong evidence guiding therapeutic decisions and this trial will address (1) whether supplemental SB is justified and (2) whether longer duration gas tamponade with C3F8 is necessary.

Detailed Description

Not available

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
560
Inclusion Criteria
  • Age ≥18 years
  • Diagnosis of rhegmatogenous retinal detachment

Exclusion Criteria, retinal detachment with:

  • Proliferative vitreoretinopathy (PVR) grade ≥C2
  • Chronic RRD with duration >3 months
  • Proliferative diabetic retinopathy with tractional retinal detachment (RD)
  • Macular holes
  • Epiretinal membrane grade 3 or 4
  • Traumatic RD
  • Giant retinal tears
  • Retinal dialysis
  • Foveoschisis
  • Wet age-related macular degeneration
  • Endophthalmitis
  • Acute retinal necrosis
  • Coats disease
  • Retinopathy of prematurity
  • Retinoschisis
  • Retinal colobomas
  • Prior glaucoma surgery or strabismus surgery (favoring PPV only)
  • Superior RD extent less than 3 clock hours (favoring PPV only)
Exclusion Criteria

Not provided

Study & Design

Study Type
INTERVENTIONAL
Study Design
FACTORIAL
Arm && Interventions
GroupInterventionDescription
Pars plana vitrectomy + sulfur hexafluoride gas tamponadeSulfur hexafluoride gas tamponade-
Pars plana vitrectomy with scleral buckle + sulfur hexafluoride gas tamponadeSulfur hexafluoride gas tamponade-
Pars plana vitrectomy with scleral buckle + perfluoropropane gas tamponadePerfluoropropane gas-
Pars plana vitrectomy + sulfur hexafluoride gas tamponadePars plana vitrectomy-
Pars plana vitrectomy + perfluoropropane gas tamponadePerfluoropropane gas-
Pars plana vitrectomy with scleral buckle + sulfur hexafluoride gas tamponadePars plana vitrectomy with scleral buckle-
Pars plana vitrectomy + perfluoropropane gas tamponadePars plana vitrectomy-
Pars plana vitrectomy with scleral buckle + perfluoropropane gas tamponadePars plana vitrectomy with scleral buckle-
Primary Outcome Measures
NameTimeMethod
Single surgery anatomic successUntil final 1 year follow-up

Freedom from reoperation for recurrent RRD

Secondary Outcome Measures
NameTimeMethod
Quality of life questionnaire2 weeks, 8-10 weeks, 6 months, 12 months
Pinhole visual acuity8-10 weeks, 6 months
Time to onset of RD recurrenceUntil final 1 year follow-up
Severity and number of complicationsUntil final 1 year follow-up
Best-corrected visual acuity1 year

Trial Locations

Locations (1)

Hôpital du Saint-Sacrement, CHU de Québec - Université Laval

🇨🇦

Québec, Quebec, Canada

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