Skip to content

Etude prospective, contrôlée, randomisée du traitement de l’occlusion sévère de la veine centrale de la rétine à sa phase précoce par injection intra-vitréenne de Bevacizumab - OVCR

Etude prospective, contrôlée, randomisée du traitement de l’occlusion sévère de la veine centrale de la rétine à sa phase précoce par injection intra-vitréenne de Bevacizumab - OVCR

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
EU CTR
Registry ID
EUCTR2009-017735-18-FR
Enrollment
Unknown
Registered
2010-04-02
Start date
2010-05-28
Completion date
Unknown
Last updated
2012-03-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

retinal vein occlusion

Interventions

Trade Name: avastin Product Name: Bevacizumab Pharmaceutical Form: Eye drops, powder and solvent for solution

Sponsors

CHRU Montpellier - Direction de la Recherche
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Age included between 18 years and 85 years OVCR recent diagnosis (=65 years) yes F.1.3.1 Number of subjects for this age range

Exclusion criteria

Exclusion criteria: Leukaemia, Myelome, Thrombophlebite, Disease of Vaquez, Disease of Osler, Disease of Behçet Amblyopic eye Diabetic maculopathie, Retinopathie diabetic Occlusion of the central artery of the associated retina (OACR) or Occlusion of the cilio-retinal artery Occlusion of branch of the central vein of the retina ( OBVCR) Other treatment of the OVCR undertaken before the inclusion

Design outcomes

Primary

MeasureTime frame
Main Objective: Evaluate the efficiency of premature covercare of the OVCR including a series of 3 intravitreal injections of Bevacizumab;Secondary Objective: Evaluation of the quality of visual function by means of a standardized questionnaire Evaluation of the oedema maculaire in OCT (Tomography in Optical Coherence) Evaluation and comparison of the tolerance of the treatment by Bevacizumab Research of complications of the OVCR;Primary end point(s): gain of visual acuteness measured in 6 months after the inclusion blind according to the international standards ETDRS and secondarily converted in acuteness logMAR.

Countries

France

Outcome results

None listed

Source: EU CTR (via WHO ICTRP) · Data processed: Feb 4, 2026