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TOPICAL INTERFERON TO TREAT UVEITIC AND PSEUDOPHAKIC MACULAR EDEMA IN A TERTIARY CARE CENTRE OF NORTHERN INDIA

Topical interferon as a newer treatment modality for uveitic and pseudophakic macular edema:A tertiary care centre study of northern india - NIL

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/10/074574
Enrollment
32
Registered
2024-10-01
Start date
Unknown
Completion date
Unknown
Last updated
2024-10-14

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

Conditions

Health Condition 1: H32- Chorioretinal disorders in diseases classified elsewhere Health Condition 2: H308- Other chorioretinal inflammations

Interventions

Intervention1: Topical interferon eyedrop: IFN eye drops were prepared from commercially available subcutaneous injection IFN 3 MU . The drug was diluted using 2.5ml of sterile water for injection to

Sponsors

Md eye hospitalMLN medical college
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: • Patients diagnosed with UME or Irvine gass syndrome and advised for intensive topical, systemic, periocular or intraocular injection of steroids or intravitreal injection of anti-VEGF, or increase in immunomodulatory therapy . • Patients already undergoing treatment for UME or P-CME and showing worsening , defined as increase in size and number of cystoid spaces and/or any increase in central macular thickness (CMT) as appreciated on SD-OCT scan after 3-4 weeks of the previous treatment.

Exclusion criteria

Exclusion criteria: 1. Patients with macular edema due to overlapping pathology other than uveitis or Irvine gass syndrome (e.g.diabetic macular edema,ARMD, choroidal neovascularisation,tumour,Central serous retinopathy,retinal vessel occlusion,post pan retinal photocoagulation ,retinitis pigmentosa). 2. Patients with any of the following ocular manifestations at the time of start of treatment- conjunctival hyperaemia,follicular hypertrophy, giant papillary conjunctivitis, irritation , corneal epithelial defect,flu like symptoms,severe dryness. 3. Patients with severe systemic disease or weight loss, deranged CBC,LFT,KFT or any mental disorder. 4. Patients with follow-up of less than one month.

Design outcomes

Primary

MeasureTime frame
Central macular thicknessTimepoint: 2weeks,4weeks,8weeks,12weeks,16weeks

Secondary

MeasureTime frame
Vision,intraocular pressureTimepoint: 2weeks,4weeks,8weeks,12weeks,16weeks

Countries

India

Contacts

Public ContactApurva bagla

Md eye hospital

drsantosh7373@gmail.com9412247373

Outcome results

None listed

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