Clinical Trials Directory

Trials / Completed

CompletedNCT01435200

Intravenous Iron in Gynecologic Cancer Patients Receiving Chemotherapy

Prevention of Blood Transfusion With Intravenous Iron in Gynecologic Cancer Patients Receiving Platinum Based Chemotherapy

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
64 (actual)
Sponsor
Chulalongkorn University · Academic / Other
Sex
Female
Age
20 Years – 70 Years
Healthy volunteers
Not accepted

Summary

Can intravenous iron lower the rate of blood transfusion in gynecologic cancer patients receiving platinum based chemotherapy than oral iron?

Detailed description

Anemia is a common condition during chemotherapy administration. Treatment options usually include oral iron supplementation and blood transfusion. However, oral iron has gastrointestinal side effects, which affects patient compliance, and only a small amount of oral iron can be absorbed from the gastrointestinal tract. Intravenous iron may overcome a block of iron absorption and iron recycling induced by hepcidin. Therefore, it may increase hemoglobin level and reduced blood transfusion in cancer patients receiving chemotherapy.

Conditions

Interventions

TypeNameDescription
DRUGIntravenous ironIntravenous iron 200 mg add in 0.9% Normal saline 100 ml infused within 15 minutes after every cycles of chemotherapy

Timeline

Start date
2011-06-01
Primary completion
2012-10-01
Completion
2012-11-01
First posted
2011-09-16
Last updated
2017-02-01

Locations

1 site across 1 country: Thailand

Source: ClinicalTrials.gov record NCT01435200. Inclusion in this directory is not an endorsement.