Trials / Withdrawn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- Withdrawn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
| Type | Name | Description |
|---|---|---|
| DIETARY_SUPPLEMENT | Iron sucrose 200 mg | I.V Iron sucrose 200 mg 2-3 times per week. Each time for 20-30 minutes |
| DIETARY_SUPPLEMENT | Iron sucrose 500 mg | I.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.