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Formulated PSTA Injection Versus PATA Alone in the Management of Macular Edema Secondary to Non-ischemic Retinal Vein Occlusions

A

Al-Azhar University

Status

Completed

Conditions

Macula Edema

Treatments

Drug: Triamcinolone Acetonide alone
Drug: Triamcinolone Acetonide and sodium hyaluronate and chondroitin sulfate

Study type

Interventional

Funder types

Other

Identifiers

NCT05385562
PSTA and macular edema

Details and patient eligibility

About

The aim of this study is to compare formulated Posterior Subtenon Triamcinolone acetonide (PSTA) injection versus Posterior Subtenon Triamcinolone acetonide alone in the management of macular edema secondary to non-ischemic retinal vein occlusions, either central or branch.

Enrollment

78 patients

Sex

All

Ages

40 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Diminution vision due to macular edema secondary to non-ischemic retinal vein occlusions, either central or branch, as evidenced by clinical and angiographic evaluation
  • CMT ≥ 250 µ.
  • Willing to participate in the study

Exclusion criteria

  • Unwilling to participate in the study.
  • Ischemic RVO
  • Prior laser treatment
  • Glaucoma/Ocular Hypertension
  • Cataract which lead to difficulty in the evaluation of macula
  • Vitreous hemorrhage
  • Macular ischemia
  • Iris neovascularisation
  • patients with intravitreal injection of anti VEGFs, steroid, or any intraocular surgery 3 months prior to the inclusion.

Trial design

Primary purpose

Treatment

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

78 participants in 2 patient groups

Formulated Posterior Sub Tenon Triamcinolone
Active Comparator group
Treatment:
Drug: Triamcinolone Acetonide and sodium hyaluronate and chondroitin sulfate
Posterior Sub Tenon Triamcinolone alone
Active Comparator group
Treatment:
Drug: Triamcinolone Acetonide alone

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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