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Somatostatin_octretide for prevention of rebleeding from gastrointestinal angiodysplasias - SOPRANO

Conditions
study to investigate the efficacy of Octeoid LAR plus standard therapy versus standard therapy alone in patients with bleeding gastrointestinal angiodysplasias
Registration Number
EUCTR2005-005313-38-DE
Lead Sponsor
Klinikum rechts der Isar, Technical University of Munich
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Recruiting
Sex
All
Target Recruitment
102
Inclusion Criteria

- patients about 18
- performed ÖGD, colosscopy or video pill
- one or more gastrotestinale haemorrage during the last three month
- detection of angiodysplasia
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

-Patients with bad general conditions
-other reasons for gastrointestinal bleeding (e. g. tumors, erosion, ulzera, varices)
-Hypertriglyceridaemie
-choledocholithiasis

Study & Design

Study Type
Interventional clinical trial of medicinal product
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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