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NCT04975074 Clinical Trial

Iron Deficiency Anemia in Twin Pregnancies

Anemia, Iron-Deficiency Clinical Trial

Official title:
Prospective Study of Iron Deficiency Anemia in Twin Pregnancy

Clinical Trial Details — Status: Not yet recruiting

Administrative data
NCT number NCT04975074
Other study ID # IDA in TP
Secondary ID
Status Not yet recruiting
Phase Phase 4
First received
Last updated
Start date July 15, 2021
Est. completion date July 2022

Study information
Verified date July 2021
Source Shengjing Hospital
Contact Fang Xie
Phone 0086-457-13604210476
Email gougou531@hotmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

All pregnant women with twin pregnancies were given oral iron according to the current recommended dose. Blood routine and ferritin were monitored during pregnancy to understand the therapeutic effect of oral iron on iron deficiency anemia and iron deficiency in pregnant women with twin pregnancies

Description:

All pregnant women with twin pregnancies were given oral iron according to the current recommended dose. Blood routine and ferritin were monitored every 2-4 weeks during pregnancy to understand the therapeutic effect of oral iron on iron deficiency anemia and iron deficiency in pregnant women with twin pregnancies.After delivery, we will test the neonatal ferritin and hemoglobin status. Our aim was to investigate the effects of iron supplementation during twin pregnancy on maternal and neonatal ferritin and anemia.

Recruitment information / eligibility
Status Not yet recruiting
Enrollment 1000
Est. completion date July 2022
Est. primary completion date December 2021
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 16 Years to 50 Years
Eligibility Inclusion Criteria: - Chinese - Pregnant women with twin pregnancies Exclusion Criteria: - Single pregnancy - Types of anemia other than iron deficiency anemia

Study Design

Related Conditions & MeSH terms

Intervention

Drug:
• Iron
One of each type of iron was taken orally according to the instructions and followed every two weeks

Locations
Country Name City State
n/a

Sponsors (1)
Lead Sponsor Collaborator
Shengjing Hospital

Outcome
Type Measure Description Time frame Safety issue
Primary Routine blood Routine blood and serum ferritin(ng/ml)were checked 2-4 weeks 2-4 weeks after antenatal care
Secondary serum ferritin routine blood and serum ferritin(ng/ml)were checked 2-4 weeks 2-4 weeks after antenatal care
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