Status:

TERMINATED

Combined Vitrectomy and Triamcinolone in Macular Edema Secondary to Branch Retinal Vein Occlusion (BRVO)

Lead Sponsor:

Helse Stavanger HF

Conditions:

Branch Retinal Vein Occlusion

Macular Edema

Eligibility:

All Genders

18+ years

Phase:

PHASE3

Brief Summary

The purpose of this study is to determine whether pars plana vitrectomy in combination with triamcinolone acetate is effective in the treatment of macular edema due to branch retinal vein occlusion.

Eligibility Criteria

Inclusion

  • Macular edema secondary to BRVO
  • Best Corrected Visual Acuity of ≤ 20/40 on ETDRS chart
  • Duration no shorter than 3 months
  • Duration no longer than 12 months

Exclusion

  • Proliferations in study eye
  • Blod in vitreous cavity
  • Previous fundus laser treatment
  • BRVO with over 180˚ of ischemia on FA
  • Age under 18
  • Other eye condition which contribute to relevant loss of visual acuity

Key Trial Info

Start Date :

November 1 2006

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

November 1 2013

Estimated Enrollment :

34 Patients enrolled

Trial Details

Trial ID

NCT00642226

Start Date

November 1 2006

End Date

November 1 2013

Last Update

January 6 2014

Active Locations (1)

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Page 1 of 1 (1 locations)

1

Stavanger University Hospital, Department of Ophthalmology

Stavanger, Norway, 4018

Combined Vitrectomy and Triamcinolone in Macular Edema Secondary to Branch Retinal Vein Occlusion (BRVO) | DecenTrialz