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CompletedNCT00373282Updated Oct 12, 2006

Triamcinolone Acetonide in Silicone-Filled Eyes as Adjunctive Treatment for Proliferative Vitreoretinopathy

A Phase 3 interventional study of Triamcinolone acetonide in Proliferative Vitreoretinopathy, sponsored by Shahid Beheshti University of Medical Sciences. Completed at 1 site in Iran, Islamic Republic of. Open to participants aged 0 Years and older. Per ClinicalTrials.gov, last updated 2006-10-12.

Sponsored by Shahid Beheshti University of Medical Sciences · Phase 3, Interventional, and Treatment

Phase
Phase 3
Study type
Interventional
Allocation
Randomized
Ages
0 Years and older
Sex
All
01

Study summary

To evaluate the effect of triamcinolone acetonide in silicone-filled eyes on the outcome of surgery for PVR.

02

Conditions studied

  • Proliferative Vitreoretinopathy

Keywords

  • PVR
  • Retinal detachment
  • Silicone oil
  • Triamcinolone
03

In context

Vitreoretinopathy, Proliferative

35 studies on the registry are indexed under Vitreoretinopathy, Proliferative; 9 are open to participants now.

Browse Vitreoretinopathy, Proliferative studies →

Lead sponsor

Shahid Beheshti University of Medical Sciences is the lead sponsor of 221 studies on the registry; 19 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
0 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Cases of rhegmatogenous retinal detachment complicated by PVR grade C undergoing vitrectomy and silicone oil tamponade.

Exclusion criteria

Exclusion Criteria:

  • History of trauma
  • Presence of diabetic retinopathy
  • History of vein occlusion
  • Giant retinal tear
05

Study design

Phase
Phase 3
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single

Interventions

  • DrugTriamcinolone acetonide
06

What researchers measure

Primary outcomes

  1. Single-operation retinal reattachment rate six

  2. months after surgery.

Secondary outcomes

  1. Visual acuity

  2. Retinal reproliferation

  3. Intraocular pressure

  4. Early silicone oil emulsification

07

Study locations

1 site
  • Hamid Ahmadieh,MD
    Tehran, 16666, Iran, Islamic Republic of
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Oct 12, 2006, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT00373282
Lead sponsor
Shahid Beheshti University of Medical Sciences
First posted
Sep 8, 2006
Start date
Jun 2001
Completion
Jun 2003
Last update
Oct 12, 2006

Study contacts

Hamid Ahmadieh, MD
principal investigator · Ophthalmic Research Center of Shaheed Beheshti Medical University
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Aug 2006. You cannot join it, but the record below documents what was studied.

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