Assesment of visual outcome post retinal detachment surgery

Not Applicable

• Conditions: Health Condition 1: H330- Retinal detachment with retinal break

• Registration Number: CTRI/2020/12/029695
• Lead Sponsor: Femin Susan Tide

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 24 November 2021

Recruitment & Eligibility

• Status: ot Yet Recruiting
• Sex: Not specified
• Target Recruitment: 0

Inclusion Criteria

(1)Unilateral RRD diagnosed by indirect ophthalmoscopy or B-scan ultrasound,

(2)Any age groups.

(3) Eyes with single surgery anatomic success is included

Exclusion Criteria

(1) Best-corrected visual acuity (BCVA) of less than 6/36 in the unaffected fellow eye due to underlying retinal disease.

(2)Postoperative macular complication, including epiretinal membrane, cystoid macular edema, macular hole.

(3)other concomitant ocular diseases (diabetic retinopathy, glaucoma, age-related macular degeneration, uveitis, retinal vascular disease, or epiretinal membrane in either eye),

(4) postoperative complications (re-detachment, proliferative vitreoretinopathy, or vitreous hemorrhage), prior vitreoretinal surgery,or prior retinal detachment in either eye

Study & Design

• Study Type: Observational
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
1.To study the correlation of visual outcomes with macular perfusion and RNFL post retinal detachment surgeryTimepoint: 4 weeks

Secondary Outcome Measures

Name	Time	Method
To evaluate the difference in macular perfusion and retinal nerve fiber layer with the fellow eye.Timepoint: 18 months