Hospital Universitario Dr Negrín
Las Palmas de Gran Canaria, Spain
NCT Number: NCT01572350
This clinical trial is designed to investigate differences in terms of efficacy (mean change in best corrected visual acuity obtained after 12 months of treatment) and safety, of 3 therapeutic estrategies for non-tractional macular edema in diabetic patients: a) laser alone; b) laser plus tiramcinolon; and c) laser plus bevacizumab.
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Notify Me18 year and older
All sexes
Interventional
Phase 3
Las Palmas de Gran Canaria, Spain
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
To be eligible, the following inclusion criteria must be met:
5.1) retinal thickening within 500 μ from the center or 5.2) hard exudates within 500 μ from the center if associated with adjacent retinal thickening or 5.3) the size of retinal thickening at least 1 area disc, part of which is less than 1 DD of the center.
A patient is not eligible if any of the following exclusion criteria are present:
Grid laser therapy acts as the standard to refer to as it is the treatment which is currently accepted by EMDDNT.
Triamcinolone 4 mg followed by modified grid laser therapy after 3-4 weeks
Other names: Triesence
Bevacizumab (1.25 mg initially, weeks 6 and 12) followed by modified grid laser therapy after3-4 weeks
Other names: Avastin
Time frame: 12 months
To evaluate the effect on best-corrected visual acuity (BCVA) of intravitreal triamcinolone (Triesence ®) or bevacizumab (Avastin ®) in combination with grid laser therapy compared to grid laser therapy alone after 12 months of treatment, in diabetic patients with not tractional diffuse macular edema (NTDDEM)
Time frame: Baseline, 3m, 6m and 12 months
Type of adverse events, severity and number of Participants with Adverse Events as a Measure of Safety and Tolerability.
Time frame: Baseline and 3, 6 and 12 months after the treatment was initiated.
To measure average change in mean central macular thickness (in microns) obtained by Optical Coherence Tomography (OCT) at each follow-up visits compared to the baseline visit in each of the three groups.
Time frame: Baseline, 3m, 6m and 12 months
Type of adverse events, severity and number of Participants with Adverse Events as a Measure of Safety and Tolerability
Time frame: Baseline, 3m, 6m and 12 months
Type of adverse events, severity and number of Participants with Adverse Events as a Measure of Safety and Tolerability
Hospital Universitario de Canarias
Other
Randomized Multicenter Clinical Trial of Three Parallel Groups to Estimate the Safety and Efficacy of Triamcinolone Acetonide Combined With Laser, Bevacizumab Combined With Laser Versus Laser Alone for the Treatment of Diffuse Non-tractional Diabetic Macular Edema.
Acronym: ALBA
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.
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