Efficacy of Octreotide on Blood and Iron Requirements in Patients With Anemia Due to Angiodysplasias
NCT02384122 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 62
Last updated 2023-05-24
Summary
The purpose of this study is to determine whether 40 mg octreotide long-acting release intramuscular every 28 days is effective in the treatment of patients with refractory anemia due to gastrointestinal angiodysplasias. We hypothesize that octreotide is effective in reducing the transfusion requirements (consisting of red blood cell transfusions and intravenous iron infusions) of patients with angiodysplasia-related anemia.
Conditions
- Angiodysplasia
- Vascular Malformations
- Gastrointestinal Hemorrhage
- Anemia
Interventions
- DRUG
-
Octreotide
Two injections of 20 mg will be given monthly.
Sponsors & Collaborators
-
Jeroen Bosch Ziekenhuis
collaborator OTHER -
Elisabeth-TweeSteden Ziekenhuis
collaborator OTHER -
Catharina Ziekenhuis Eindhoven
collaborator OTHER -
Bernhoven Hospital
collaborator OTHER -
Tjongerschans hospital
collaborator UNKNOWN -
Gelre Hospitals
collaborator OTHER -
Maasstad Hospital
collaborator OTHER -
Reinier de Graaf Groep
collaborator OTHER -
University Medical Center Groningen
collaborator OTHER -
Rijnstate Hospital
collaborator OTHER -
St. Antonius Hospital
collaborator OTHER -
Radboud University Medical Center
lead OTHER
Principal Investigators
-
Joost Drenth, MD. PhD · Radboud University Medical Center
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- SINGLE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2015-09-30
- Primary Completion
- 2022-07-31
- Completion
- 2023-05-31
Countries
- Netherlands
Study Locations
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