Comparison of Conventional vs Wide Angle Viewing System for Scleral Buckling Surgery

Randomized Controlled Trial for comparing Conventional vs Wide Angle Viewing System for Scleral Buckling Surgery

Status

Active, not recruiting

Phases

Phase 4

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2022/03/040706

Enrollment

Registered

2022-03-02

Start date

Unknown

Completion date

Unknown

Last updated

2022-04-04

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

Conditions

Health Condition 1: O- Medical and Surgical

Interventions

Intervention1: Scleral Buckling Surgery using Wide Angle Non Contact Viewing System with Chandelier Illuminator: The study will consist of 46 subjects with rhegmatogenous retinal detachment who will b

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients presenting with rhegmatogenous retinal detachment. 2. Planned for scleral buckle surgery under local/general anaesthesia. 3. Patients ready for a 3 month follow up

Exclusion criteria

Exclusion criteria: 1. Patients with proliferative vitreoretinopathy > grade C. 2. Patients with giant retinal tears. 3. Patients with significant media opacity excluding good fundus visualization. 4. Patients with posterior retinal breaks. 5. Post glaucoma surgery/ patient with glaucoma drainage implant.

Design outcomes

Primary

Measure	Time frame
Primary anatomical success i.e., complete reattachment of the retinaTimepoint: Assessment at 1 week and 1 month	—

Secondary

Measure	Time frame
Best-corrected visual acuity (BCVA) in logMARTimepoint: Assessment at 1 and 3 months;Perioperative and postoperative complicationsTimepoint: Assessment at 1 and 3 months	—

Countries

India

Contacts

Public ContactDr Sanjiv Kumar Gupta

King Georges Medical University, Lucknow

sanjiv204@gmail.com7905613731

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026