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Completed Phase 4 Interventional

Effect of Iron Therapy as an Adjunct to Epoetin Alfa in the Anemia of Cancer Chemotherapy

ClinicalTrials.gov ID: NCT00224068

Public ClinicalTrials.gov record NCT00224068. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jul 21, 2026, 11:20 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Multicenter, Randomized, Controlled Prospective Trial of the Safety and Efficacy of Ferrlecit® in Anemic Cancer Patients Who Are Receiving Acute Chemotherapy and Epoetin as Compared to Oral Iron and No Treatment

Study identification

NCT ID
NCT00224068
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Lead sponsor
Watson Pharmaceuticals
Industry
Enrollment
180 participants

Conditions and interventions

Conditions

Interventions

  • Sodium ferric gluconate, ferrous sulfate, standard of care Drug

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Apr 30, 2002
Primary completion
Nov 30, 2003
Completion
Nov 30, 2003
Last update posted
Mar 1, 2012

2002 – 2003

United States locations

U.S. sites
32
U.S. states
22
U.S. cities
32
Facility City State ZIP Site status
Not listed Bakersfield California
Not listed Chula Vista California
Not listed Long Beach California
Not listed Los Angeles California
Not listed Norwich Connecticut
Not listed Port Saint Lucie Florida
Not listed Zephyrhills Florida
Not listed Columbus Georgia
Not listed Coeur d'Alene Idaho
Not listed Hutchinson Kansas
Not listed Lexington Kentucky
Not listed Baton Rouge Louisiana
Not listed Baltimore Maryland
Not listed Detroit Michigan
Not listed Saint Joseph Michigan
Not listed Southfield Michigan
Not listed Duluth Minnesota
Not listed Greenwood Mississippi
Not listed Cherry Hill New Jersey
Not listed Denville New Jersey
Not listed Manhasset New York
Not listed Bismarck North Dakota
Not listed Columbus Ohio
Not listed Philadelphia Pennsylvania
Not listed Pittsburgh Pennsylvania
Not listed West Chester Pennsylvania
Not listed Columbia South Carolina
Not listed Laredo Texas
Not listed Richmond Virginia
Not listed Salem Virginia
Not listed Walla Walla Washington
Not listed Milwaukee Wisconsin

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00224068, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Mar 1, 2012 · Synced Jul 21, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00224068 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →