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NCT03883841 Clinical Trial

Fetal Vascular Hemodynamic Changes in Iron Deficiency Anemia

Iron Deficiency Anemia Clinical Trial

Official title:
Fetal Vascular Hemodynamic Changes Before and After Treatment of Maternal Iron Deficiency Anemia

Clinical Trial Details — Status: Not yet recruiting

Administrative data
NCT number NCT03883841
Other study ID # DIDA
Secondary ID
Status Not yet recruiting
Phase
First received
Last updated
Start date May 2019
Est. completion date October 2020

Study information
Verified date March 2019
Source Assiut University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Iron deficiency anemia is a worldwide medical disorder. So far, it is the most common medical complication in pregnancy specially in developing countries. It is the cause of many adverse effects on mother and fetus and contributes significantly to high maternal mortality. Maternal iron deficiency anemia is frequently associated with premature delivery, low birth weight babies

Recruitment information / eligibility
Status Not yet recruiting
Enrollment 60
Est. completion date October 2020
Est. primary completion date August 2020
Accepts healthy volunteers No
Gender Female
Age group N/A and older
Eligibility Inclusion Criteria:

- Pregnant women with gestational age 28-32 weeks

- singleton pregnancy

- iron deficiency anemia.

Exclusion Criteria:

- Multiple pregnancy

- antepartum hemorrhage

- major congenital fetal anomalies

- any other type of anemia other than iron deficiency anemia

- any acute or chronic maternal disease other than iron deficiency anemia.

Study Design

Related Conditions & MeSH terms

Intervention

Drug:
• Iron Sucrose Solution for Injection
intravenous infusion of iron sucrose

Locations
Country Name City State
n/a

Sponsors (1)
Lead Sponsor Collaborator
Assiut University

Outcome
Type Measure Description Time frame Safety issue
Primary The mean changes in middle cerebral artery Doppler of the fetus Doppler evaluation one month
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