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Ozurdex for patients with macular edema secondary to intraocular vasular tumors

A Prospective Study of Dexamethasone (Ozurdex) Posterior Segment Drug Delivery System in the Treatment of Patients with Cystoid Macular Edema Secondary to Intraocular Vascular Tumors.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/11/038270
Enrollment
25
Registered
2021-11-25
Start date
Unknown
Completion date
Unknown
Last updated
2022-02-21

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

Conditions

Health Condition 1: H318- Other specified disorders of choroid

Interventions

Intervention1: Intravitreal dexamethasone implant: 0.7 mg biodegradeble intravitreal implant Control Intervention1: NA: NA

Sponsors

LV Prasad Eye Institute
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Newly diagnosed patients with CME secondary to intraocular vascular tumors 2.Participant is willing and able to give informed consent for participation in the study. 3.Male and Female, aged 10 years or above. 4.BCVA 20/32 to 20/400 inclusive 5.Central subfoveal OCT thickness > 300 microns

Exclusion criteria

Exclusion criteria: 1.Any co-existing ocular disease other than intraocular tumor which might cause macular edema. 2.Intraocular surgery within 3 months 3.History of IOP elevation in response to steroid treatment in either eye. 4.History of glaucoma or optic nerve head change consistent with glaucoma damage, and/or glaucomatous visual field loss in the study eye.

Design outcomes

Primary

MeasureTime frame
1.BCVA as per ETDRS chart (distance & near acuity) 2.Central subfoveal thickness on OCT 3.Wide-field fundus photograph 4.B scan to document the tumor dimensions 5. IOP Timepoint: 3 months & 6 months

Secondary

MeasureTime frame
1. BCVA as per ETDRS chart (distance & near acuity) 2. Central subfoveal thickness on OCT 3. Wide-field fundus photograph 4. B scan to document the tumor dimensions 5. IOP Timepoint: 3 months,6 months

Countries

India

Contacts

Public ContactDrVishal Raval

LV Prasad Eye Institute

drvishalraval@gmail.com08374588011

Outcome results

None listed

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