Viewing Study NCT00224042



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Last Modification Date: 2024-10-26 @ 9:19 AM
Study NCT ID: NCT00224042
Status: COMPLETED
Last Update Posted: 2012-03-29
First Post: 2005-09-13

Brief Title: Effect of Ferrlecit Versus Oral Iron on Iron Deficient Chronic Kidney Disease CKD Patients Receiving Erythropoietic Agents
Sponsor: Watson Pharmaceuticals
Organization: Watson Pharmaceuticals

Study Overview

Official Title: A Randomized Controlled Open-label Study of the Safety and Efficacy of Ferrlecit vs Oral Iron in Iron Deficient Patients With Chronic Kidney Disease Being Treated With Erythropoietic Therapy
Status: COMPLETED
Status Verified Date: 2012-02
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: This study compares the effect of Ferrlecit a form of intravenous iron to ferrous sulfate a form of oral iron in treating anemia and iron deficiency in chronic kidney disease patients who are receiving erythropoietic agents such as Procrit and Aranesp
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None