Longterm Efficiency and Safety of Intravitreal Injections With Bevacizumab in Patients With Neovascularisation or Macular Edema

Who is this study for? Patients with Retinal Neovascularization, Macular Edema
What treatments are being studied? Bevacizumab Injection [Avastin]
Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 4
SUMMARY

Although the safety and efficacy of bevacizumab has been established in several phase 3 trials, there is only little documented about the long-term safety and efficacy in the 'real-world practice' in large populations from different regions. Therefore the investigators evaluate the long-term safety and efficacy of intravitreal treatment with bevacizumab by registration of best corrected visual acuity, side-effects and central retinal thickness as measured with the ocular coherence tomography if available. This will allow the investigators to compare the results of their centre with the results of several phase 3 trials from the literature and will guide improvements in their treatment protocols.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Age ≥ 18 years of either gender

• Written informed consent must be obtained before any intravitreal injection of bevacizumab is performed

• Visual impairment predominantly due to abnormal new vessel ingrowth and/or macular edema. The presence of fluid (intraretinal, subretinal or sub-RPE) detected clinically or on the ocular coherence tomography.

⁃ If both eyes are eligible for the study, both eyes can be included in the study.

Locations
Other Locations
Belgium
Ghent University Hospital
RECRUITING
Ghent
Contact Information
Primary
Julie De Zaeytijd, MD
julie.dezaeytijd@ugent.be
+32 9 332 26 29
Time Frame
Start Date: 2013-11-22
Estimated Completion Date: 2024-12-31
Participants
Target number of participants: 500
Treatments
Other: open label
Sponsors
Leads: University Hospital, Ghent

This content was sourced from clinicaltrials.gov