Clinical Trials Directory

Trials / Completed

CompletedNCT05345808

Efficacy of Formulated Posterior Sub Tenon Triamcinolone in Macular Edema Secondary to Non-Ischemic Retinal Vein Occlusions

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
46 (actual)
Sponsor
Al-Azhar University · Academic / Other
Sex
All
Age
50 Years – 69 Years
Healthy volunteers
Not accepted

Summary

Retinal vein occlusion (RVO) is considered the second vascular disorder of the retina after diabetic retinopathy. Patients with RVO are at risk of the development of macular edema. Different treatment modalities for macular edema include LASER therapy, antivascular endothelial growth factor (VEGF), and triamcinolone. Aim To detect the efficacy of formulated Triamcinolone Acetonide(TA) injection in the posterior subtenon space to manage macular edema secondary to non-ischemic RVOs, either central or branch.

Conditions

Interventions

TypeNameDescription
DRUGTriamcinolone AcetonideTriamcinolone Acetonide formulated with chondroitin sulfate and sodium hyaluronate

Timeline

Start date
2021-03-01
Primary completion
2022-02-20
Completion
2022-03-30
First posted
2022-04-26
Last updated
2022-04-26

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT05345808. Inclusion in this directory is not an endorsement.