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Randomized, placebo controlled, patient and observer masked study to evaluate the efficacy of treatment with Sandostatin LAR 20 mg i.m. or placebo every 4 weeks during 6 months in 120 patients with exudative age-related macular degeneration.

Completed
Registration Number
NL-OMON25954
Brief Summary

T.Missotten, G.S. Baarsma, R.W. A. M. Kuijpers, P.M. van Hagen. Somatostatin Analog for the Treatment of Exsudative Age Related Macular Degeneration: A Randomised Trial. ARVO 2007.

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
120
Inclusion Criteria

1. Recent history of visual acuity decrease (< 6 weeks prior to study start) related to exudative ARMD;

2. Clinical signs of ARMD (i.e. drusen and/or RPE changes);

Exclusion Criteria

1. Diabetes mellitus;

2. Symptomatic cholelithiasis;

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Visual acuity and contrast sensitivity,<br>decrease in macular edema and arrest of neovascularisation (FAG).
Secondary Outcome Measures
NameTimeMethod
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