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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04183829
Other study ID # No.2018-I2M-1-004
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date June 1, 2019
Est. completion date June 2022

Study information

Verified date June 2019
Source National Research Institute for Family Planning, China
Contact Tu Pengcheng, M.D.
Phone +86 18810266933
Email manutu@126.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

A prospective multicenter cohort study to evaluate effects of prior induced termination of pregnancy on complications and pregnancy outcomes.


Description:

A prospective multicenter cohort study to evaluate effects of prior induced termination of pregnancy on complications and pregnancy outcomes.


Recruitment information / eligibility

Status Recruiting
Enrollment 20000
Est. completion date June 2022
Est. primary completion date June 2020
Accepts healthy volunteers
Gender Female
Age group 18 Years to 40 Years
Eligibility Inclusion Criteria:

- women have induced abortion in early pregnancy (<12 weeks of gestation).

- permanent population and no tendency to move.

- normal language expression and understanding ability, able to understand research content.

- be able and willing to provide written informed consent and effective contact information, and be willing to cooperate with follow-up investigations.

Exclusion Criteria:

- above the age of 40

- with history of adverse pregnancy and childbirth

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
induced termination of pregnancy
Medically, induced termination of pregnancy (I-TOP) is defined as an intervention to voluntarily terminate a pregnancy (ie, induced abortion) by either surgical or medical means so it does not result in a live birth.

Locations

Country Name City State
China Changzhou Maternal and Child Health Hospital Changzhou Jiangsu
China Daqing People's Hospital Daqing Heilongjiang
China People's Hospital of Inner Mongolia Autonomous Region Hohhot Mongolia Autonomous
China Qingdao Maternal and Child Health Hospital Qingdao Shandong
China Taiyuan Maternal and Child Health Hospital Taiyuan Shanxi
China Tanggu Maternal and Child Health Hospital Tanggu Tianjin
China Yangzhou Maternal and Child Health Hospital Yangzhou Jiangsu
China Zaozhuang Maternal and Child Health Hospital Zaozhuang Shandong
China Zhangjiakou Maternal and Child Health Hospital Zhangjiakou Hebei
China Zhongshan Boai Hospital Zhongshan Guangdong

Sponsors (1)

Lead Sponsor Collaborator
National Research Institute for Family Planning, China

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary adverse pregnancy outcomes the rate of different adverse pregnancy outcomes 2021.6
Secondary Complications the rate of different complications 2020.6
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