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NCT06044181

Peripheral Avascular Retina in Retinopathy of Prematurity

Status unknown NA Last updated 13 May 2024
What this trial tests

NA trial testing Diode laser photocoagulation. in Retinopathy of Prematurity in 32 participants. Status unknown.

Timeline
1 January 2024
Primary endpoint
1 May 2025
1 November 2025

Quick facts

Lead sponsorAssiut University
PhaseNA
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationnon randomized
Designparallel
Maskingnone
Primary purposetreatment
Enrollment32
Start date1 January 2024
Primary completion1 May 2025
Estimated completion1 November 2025
Sites1 location across Egypt

Drugs / interventions tested

Conditions studied

Sponsor

Assiut University

Who can join

Adults 18 Months to 3, any sex, with Retinopathy of Prematurity. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Retinopathy of prematurity (ROP) is a widely known retinal vascular disorder in preterm infants and a leading cause of visual disability or blindness in children. Advances in antenatal care have resulted in an increase in the survival rate of infants with extremely low birth weight (BW). Approximately 90% of infants who develop ROP do so by a postmenstrual age of 46.3 weeks. In certain patients with or without treatment, the retina may fail to fully vascularize or may develop vascular abnormalities, thus demonstrating persistent avascular retina (PAR) or anomalous vessel findings at the periphery. Because of the advent of technologies such as ultrawide-field fluorescein angiography (UWFFA) persistent vascular abnormalities can be detected more readily and investigated.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Retinopathy of Prematurity

Currently open trials in the same condition.

Other Assiut 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/NCT06044181.

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