Maintenance Treatment of Iron Deficiency in IBD Patients

NCT00810004 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 245

Last updated 2012-12-21

No results posted yet for this study

Summary

The aim of this study is to evaluate the treatment of iron deficiency in IBD patients.

Conditions

Interventions

DRUG

Ferinject

Intravenous infusion of iron

Sponsors & Collaborators

  • Parexel

    collaborator INDUSTRY
  • Vifor Pharma

    lead INDUSTRY

Principal Investigators

  • Christoph Gasche, Professor · Medical University of Vienna

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2009-02-28
Primary Completion
2010-10-31
Completion
2010-10-31

Countries

  • Russia

Study Locations

More Related Trials

Entities

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 NCT00810004 on ClinicalTrials.gov