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NCT05712642

A Dosing Study of Intravitreal Bevacizumab for Retinopathy of Prematurity

Completed Phase 3 Last updated 3 February 2023
What this trial tests

Phase 3 trial testing Intravitreal Bevacizumab in Retinopathy of Prematurity in 19 participants. Completed in 28 January 2021.

Timeline
1 February 2020
Primary endpoint
30 December 2020
28 January 2021

Quick facts

Lead sponsorCairo University
PhasePhase 3
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingdouble
Primary purposetreatment
Enrollment19
Start date1 February 2020
Primary completion30 December 2020
Estimated completion28 January 2021
Sites1 location across Egypt

Drugs / interventions tested

Conditions studied

Sponsor

Cairo University

Who can join

Adults 28 Weeks to 40 Weeks, any sex, with Retinopathy of Prematurity. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The aim of our study was to determine whether a low dose of 0.3125mg intravitreal bevacizumab is effective in treatment of type 1 ROP as the standard 0.625 mg dose., regarding : Serum Systemic VEGF levels. Retinal Vascularization.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other recruiting trials for Retinopathy of Prematurity

Currently open trials in the same condition.

Other Cairo University trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05712642.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing