Clinical Trials Directory

Trials / Withdrawn

WithdrawnNCT02441439

To Compare the Efficacy of I.V 200 mg Iron Sucrose and 500 mg Iron Sucrose to Treat Anemia in Pregnancy

Status
Withdrawn
Phase
N/A
Study type
Interventional
Enrollment
0 (actual)
Sponsor
HaEmek Medical Center, Israel · Academic / Other
Sex
Female
Age
18 Years
Healthy volunteers
Not accepted

Summary

This study is aimed to compare the efficacy of 2 doses of iron sucrose given intravenously - 200 mg versus 500 mg.

Detailed description

Anemia is common during pregnancy. It is associated with maternal and neonatal complications. It is acceptable to prescribe oral iron supplements. However, gastrointestinal side effects are very common and those lead to patient's intolerance as well as low patient's compliance. In those cases, as well as in severe anemia it is recommended to give iron sucrose. This drug is administered intravenously is effective to treat iron deficiency anemia with a minimal adverse effect profile. The two methods of giving iron sucrose is (1) to give I.V 200 mg iron sucrose 2-3 times/week or (2) to give I.V 500 mg iron sucrose once a week In the present study we aim to compare between the efficacy of those 2 protocols.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTIron sucrose 200 mgI.V Iron sucrose 200 mg 2-3 times per week. Each time for 20-30 minutes
DIETARY_SUPPLEMENTIron sucrose 500 mgI.V Iron sucrose 500 mg once per week. Each time for 3.5 hours

Timeline

Start date
2022-01-01
Primary completion
2022-11-07
Completion
2022-11-07
First posted
2015-05-12
Last updated
2022-11-08

Source: ClinicalTrials.gov record NCT02441439. Inclusion in this directory is not an endorsement.