Skip to main content
OpenTrials
Completed

NCT Number: NCT02308644

Intravitreous Bevacizumab and Standard Metabolic Control for Diabetic Macular Edema - A Contrast Sensitivity Study

To evaluate the effects on contrast sensitivity (CS) measurements of intravitreal bevacizumab injections associated with standard metabolic control in eyes with diabetic macular edema (DME) associated with standard metabolic control.

Completed

Looking for future studies?

Notify Me

Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 3

Primary location

University of Sao Paulo

São Paulo, 05403-000, Brazil

About this study

Prospective, randomized, masked and interventional study. Patients with diabetes mellitus (DM) 2, glycated hemoglobin (HbA1c) less than 11% and previously treated macular edema three months before will be randomized in two groups. The baseline examination consisted of visual acuity (VA), CS using the Pelli-Robson Charts, optical coherence tomography (OCT) and Fluorescein Angiography for all eyes.

The same tests will be repeated above, in both groups, again, in the week 2,6 and 12, when the data is then collected for analysis and so ended the closed phase. On the same day will start the open phase, which will be applied intravitreal injection of bevacizumab in both groups and the same tests of closed phase will be held in the week 14,18 and 24 when the study will be completed then [Table 1] .

Patients will be monitored and controlled clinically including blood pressure measurements, laboratory blood tests such as blood glucose, glycated hemoglobin, urea, creatinine, total cholesterol and fractions.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Age at least 18 years old, of both genders;
  • Patients with diabetes mellitus type I or type II;
  • Macular edema presence of clinically significant diabetic in their mixed or diffuse;
  • Visual acuity worse than 20/40 corrected (< 68 letters ETDRS)
  • Glycated hemoglobin ≤ 11%;
  • Systolic and diastolic blood pressure < 170 and < 100 mmHg, respectively;
  • Women not pregnant;
  • Free and informed consent term signed the screening visit;
  • Ability to adhere to the visits.

Exclusion criteria

  • Failure to comply with any of the inclusion criteria;
  • Treatment for DME within the prior 3 months;
  • Vitreoretinal traction within 1 disc diameter (DD) of the fovea, clinically confirmed or with OCT;
  • Atrophy or fibrosis surrounding the fovea;
  • Any level of cataract;
  • Vitreous hemorrhage or any opacity means;
  • Eye disease related to diabetic retinopathy that can derail the central vision (eg Age Macula Degeneration, chorioretinitis scar, ...)
  • Best-corrected visual acuity to 20/40 (> 68 letters ETDRS)
  • Inability to understand the treatment and the term of consent;
  • Debilitating systemic disorders that preclude the patient's admission to the study, according to the clinical judgment of the investigator;

Treatment and study plan

intravitreal bevacizumab injection(1.25mg)

Drug

intravitreal bevacizumab injection(1.25mg) / Sham injection

Other names: Avastin, Genentech Inc., South San Francisco, CA, EUA

Primary outcomes

  1. Contrast sensitivity

    Time frame: 6 months (24 weeks )

    Evaluate the Contrast Sensitivity measured by Pelli-Robson charts (Clement Clarke Inc., Columbus, OH) at baseline, weeks 2,6,12,14,18 and 24 to be compared with visual acuity gold standard - Early Treatment of Diabetic Retinopathy Study - ETDRS charts

Secondary outcomes

  1. Metabolic control

    Time frame: 6 months (24 weeks)

    Evaluate the effects of the standard metabolic control with glycated hemoglobin (HbA1c) levels in eyes with diabetic macular edema, measured by method certified by National Glycohemoglobin Standardization Program (NGSP) / reference values = 4.1 a 6.5%).

Sponsors and collaborators

Lead sponsor

University of Sao Paulo

Other

Registry information

Official study title

Phase 3 Intravitreous Bevacizumab and Standard Metabolic Control for Diabetic Macular Edema - A Contrast Sensitivity Pilot Study.

Important dates

Study start
2009
Primary completion
2011
Study completion
2013
First posted
Dec 4, 2014
Registry last updated
Dec 4, 2014

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.