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Treatment of neovascular age related macular degeneration with intravitreal Bevacizumab (Avastin)

Treatment of neovascular age related macular degeneration with intravitreal Bevacizumab (Avastin)

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
EU CTR
Registry ID
EUCTR2006-001914-34-DE
Enrollment
Unknown
Registered
2006-05-08
Start date
2006-08-30
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

neovascular age-related macular degeneration

Interventions

Trade Name: Avastin 25 mg/ml Pharmaceutical Form: Solution for injection INN or Proposed INN: Bevacizumab Concentration unit: mg/ml milligram(s)/millilitre Concentration number: 25-

Sponsors

Bert Mueller, Dep. Ophthalmology
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients older than 50 years, neovascular age related macular degeneration, loss of visual acuity within 3 months prior to inclusion Are the trial subjects under 18? no Number of subjects for this age range: F.1.2 Adults (18-64 years) yes F.1.2.1 Number of subjects for this age range F.1.3 Elderly (>=65 years) yes F.1.3.1 Number of subjects for this age range

Exclusion criteria

Exclusion criteria: allergy to bevacizumab, contraindication to bevacizumab (unstable Angina pectoris, recent myocardial infarction and stroke), other ocular disease

Design outcomes

Primary

MeasureTime frame
Primary end point(s): primary endpoint: loss of more than 15 letters ;Main Objective: To test effeciacy and safety of 1mg intravitreal Bevacizumab in patients with neovascular age related macular degeneration and recent loss of visual acuity ;Secondary Objective: to test reading velocity, contrast sensitivity, visual fixation ability, vascular permeability, quality of life questionaire,

Countries

Germany

Outcome results

None listed

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