Trial Details

Not recruiting
Basic Information
Clinical ID c3309
Identifier NCT00810004
Trial Title A Multi-centre, Randomised, Prospective, Single-blinded, Controlled Study to Investigate the Efficacy and Safety of a Standardised Maintenance Dosage Regimen of Intravenous Ferric Carboxymaltose (FERINJECT) Versus Placebo in Patients With Iron Deficiency Caused by Inflammatory Bowel Disease
Trial URL Visit Original Page
Study Information
Study Results

No results available

Conditions Iron Deficiency;Inflammatory Bowel Disease
Interventions Drug: Ferinject
Participant Information
Sponsor Vifor Inc.
City -
Country/Region Russia
Enrollment Criteria
Sex Requirement ALL
Age Requirement -
Study Design
Study Type Interventional
Phase PHASE3
Time Information
Start Date 2025-04-24
Primary Completion Date -
Completion Date -