Skip to main content
OpenTrials
Completed

NCT Number: NCT00737971

Efficacy Study of Triamcinolone and Bevacizumab Intravitreal for Treatment of Diabetic Macular Edema

Triamcinolone and Bevacizumab Intravitreal for Treatment of Diabetic Macular Edema

Completed

Looking for future studies?

Notify Me

Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

Federal University of Sao Paulo - Dept. of Ophthalmology / Vision Institute

São Paulo, 04040-002, Brazil

About this study

Efficacy Study of Triamcinolone and Bevacizumab Intravitreal for Treatment of Diabetic Macular Edema

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 18 years of age at least
  • Diagnosis of diabetes mellitus (type 1 or type 2. any one of the following will be considered to be sufficient evidence that diabetes is present:
  • current regular use of insulin for the treatment of diabetes
  • current regular use of oral hypoglycemic agents for the treatment of diabetes
  • diabetes as defined by american Diabetes Association (ADA)
  • symptoms of diabetes (polyuria, polydipsia, and unexplained weight loss) or eighth-hour fasting plasma glucose > 126 mg/dl
  • Diabetic macular edema clinically observable associated with diabetic retinopathy:
  • without prior foveal treatment with laser therapy
  • if photocoagulation or peripherical or macular laser, at least 3 months
  • absence of macular ischemia by fluorescein angiography on baseline visit
  • BCVA score between 20 letters (20/400 ETDRS)e 70 letters (20/40 ETDRS) in the study eye measured by the ETDRS method at qualification/baseline visit
  • Retinal thickness > 275um by OCT
  • One eye per patient will be chosen for the study. In case of both eye eligible, it will be chosen an eye to be treated with study medication and another eye treated with laser
  • Taught hyaloid syndrome

Exclusion criteria

  • Uncontrolled systemic disease
  • Initiation of medical therapy for diabetes or a change from oral hypoglycemic agents to insulin therapy within 4 months prior to the qualification visit
  • Renal failure requiring hemodialysis or peritoneal dialysis within 6 months prior to the qualification visit
  • Any ocular condition in the study eye that in the opinion of the investigator would prevent a 2 lines improvement of visual acuity (e.g. severe macular ischemia)
  • Presence of branch retinal vein occlusion, central retinal vein occlusion, uveitis, pseudophakic cystoid edema or any other condition in the study eye which could be contributing to macular edema
  • Presence of an epiretinal membrane in the study eye
  • History of IOP elevation in response to steroid treatment in either eye
  • History of glaucoma or optic nerve head change consistent with glaucoma damage
  • Ocular hypertension requiring more than 1 anti-glaucoma medication to maintain IOP < 11mmhg at qualification visit
  • Presence of anterior chamber intraocular lens in the study eye
  • Active optic disc or retinal neovascularization in the study eye at qualification visit
  • Active or history of choroidal neovascularization in the study eye

Treatment and study plan

Bevacizumab intravitreal

Drug

Bevacizumab intravitreal 0.05 ml/1.25 mg - administered on D0, Week 4, Week 8

Other names: Avastin

Triamcinolone

Drug

Intravitreal 0.1 ml/4 mg, D0, Week 4 and Week 8

Triamcinolone + Bevacizumab

Drug

Intravitreal triamcinolone 0.1 ml/4 mg + bevacizumab 0.05 ml/1.25 mg simultaneously on D0, week 4, Week 8

Other names: triamcinolone + avastin

Primary outcomes

  1. Measurement of visual acuity (E Snellen)

    Time frame: monthly

Secondary outcomes

  1. Tonometry

    Time frame: monthly

  2. Measurement of retinal thickness by OCT

    Time frame: monthly

Sponsors and collaborators

Lead sponsor

Rubens Belfort Jr.

Other

Registry information

Official study title

A Randomized, Parallel Group, Masked Clinical Study to Evaluate the Efficacy of Triamcinolone and Bevacizumab Through Intravitreal Injection With Individual or Simultaneous Drugs to Treatment of Diabetic Macular Edema

Acronym: ATEMD

Important dates

Study start
2008
Primary completion
2012
Study completion
2013
First posted
Aug 20, 2008
Registry last updated
May 3, 2016

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.