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Efficacy of intravitreal brolucizumab in choroidal neovascularisation

Efficacy of intravitreal brolucizumab in choroidal neovascularisation an industrial hospital based prospective interventional study - NIL

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/05/086622
Enrollment
43
Registered
2025-05-09
Start date
Unknown
Completion date
Unknown
Last updated
2025-05-26

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

Conditions

Health Condition 1: H309- Unspecified chorioretinal inflammation

Interventions

Intervention1: Brolucizumab: single dose of 0.05 mL containing 6 mg. Pro Re Nata frequency each 4 weeks Control Intervention1: NIL: NIL

Sponsors

Anuj Sanjay Pawar
Lead Sponsor
Chitra Sunov
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: Newly diagnosed CNV patients of any cause with involvement of central macula or within 500 microns of the macula.

Exclusion criteria

Exclusion criteria: Already treated cases Visually significant cataract Pregnancy History of CVA, myocardial infarction within three months CKD Stage 4 onwards patients, diabetic nephropathy One eyed patient

Design outcomes

Primary

MeasureTime frame
Resolution of macular fluid, as determined by OCT, Improvement in Best corrected Visual AcuityTimepoint: Resolution of macular fluid, as determined by OCT, Improvement in Best corrected Visual Acuity at 4 weeks, 8 weeks, 12 weeks, 16 weeks, 24 weeks, 36 weeks, 48 weeks, 60 weeks 72 weeks

Secondary

MeasureTime frame
MEASUREMENT IN mean best-corrected visual acuity (BCVA) change from baseline to Week 72 (margin: 4 letters). Other key end points included the percentage of patients who maintained q12w dosing through Week 72 and anatomic outcomes.Timepoint: WEEK 48, WEEK 72

Countries

India

Contacts

Public ContactAnuj Sanjay Pawar

Jawaharlal nehru hospital and reserach centre sector 9 bhilai

csunov@gmail.com7447519449

Outcome results

None listed

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