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

No results posted yet for this study

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

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02384122 on ClinicalTrials.gov