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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT04486456
Other study ID # ERIC STUDY
Secondary ID
Status Not yet recruiting
Phase
First received
Last updated
Start date August 2020
Est. completion date December 2022

Study information

Verified date July 2020
Source Peking University First Hospital
Contact Song X Zhang
Phone 13901024399
Email 1033341681@qq.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The purpose of this study is to describe the prevalence of anemia and iron deficiency in pregnancy through a multi-center, prospective follow-up study . To explore the influence factors of anemia and iron deficiency in pregnancy; to explore the influence of anemia and iron deficiency in pregnancy on maternal and fetal outcomes.


Description:

1. To understand the epidemiological characteristics of anemia and iron deficiency in pregnancy and describe the epidemiological situation of anemia and iron deficiency.

2. To explore the influence factors of anemia and iron deficiency in pregnancy.

3. To explore the influence of anemia and iron deficiency during pregnancy on the pregnancy outcome of mothers and infants.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 20000
Est. completion date December 2022
Est. primary completion date August 2022
Accepts healthy volunteers
Gender Female
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Regular prenatal check-ups were conducted in the hospitals participating in the study, and pregnant women who planned to give birth in hospital were established a maternity health manual

- 18 years and older

- Patients have to agree to participate by signing a consent

Exclusion Criteria:

- have severe chronic diseases with Pre-pregnancy

- Suffer from severe mental illness

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Peking University First Hospital

Outcome

Type Measure Description Time frame Safety issue
Primary Hb Proportion of patients with Hb<110g/L Completed by observation,an average of 1 year
Secondary SF Proportion of patients with SF<20µg/L Completed by observation,an average of 1 year
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