- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04183829
Effects of Prior Induced Termination of Pregnancy on Complications and Pregnancy Outcomes.
November 28, 2019 updated by: National Research Institute for Family Planning, China
A prospective multicenter cohort study to evaluate effects of prior induced termination of pregnancy on complications and pregnancy outcomes.
Study Overview
Status
Unknown
Conditions
Intervention / Treatment
Detailed Description
A prospective multicenter cohort study to evaluate effects of prior induced termination of pregnancy on complications and pregnancy outcomes.
Study Type
Observational
Enrollment (Anticipated)
20000
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Tu Pengcheng, M.D.
- Phone Number: +86 18810266933
- Email: manutu@126.com
Study Locations
-
-
Guangdong
-
Zhongshan, Guangdong, China
- Recruiting
- Zhongshan Boai Hospital
-
-
Hebei
-
Zhangjiakou, Hebei, China
- Recruiting
- Zhangjiakou Maternal and Child Health Hospital
-
Contact:
- Tu Pengcheng, M.D.
-
-
Heilongjiang
-
Daqing, Heilongjiang, China, 150000-160000
- Recruiting
- Daqing People's Hospital
-
Contact:
- Tu Pengcheng, M.D.
-
-
Jiangsu
-
Changzhou, Jiangsu, China
- Recruiting
- Changzhou Maternal and Child Health Hospital
-
Yangzhou, Jiangsu, China
- Recruiting
- Yangzhou Maternal and Child Health Hospital
-
-
Mongolia Autonomous
-
Hohhot, Mongolia Autonomous, China
- Recruiting
- People's Hospital of Inner Mongolia Autonomous Region
-
Contact:
- Tu Pengcheng, M.D.
-
-
Shandong
-
Qingdao, Shandong, China
- Recruiting
- Qingdao Maternal and Child Health Hospital
-
Zaozhuang, Shandong, China
- Recruiting
- Zaozhuang Maternal and Child Health Hospital
-
-
Shanxi
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Taiyuan, Shanxi, China
- Recruiting
- Taiyuan Maternal and Child Health Hospital
-
-
Tianjin
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Tanggu, Tianjin, China
- Recruiting
- Tanggu Maternal and Child Health Hospital
-
Contact:
- Tu Pengcheng, M.D.
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 40 years (Adult)
Accepts Healthy Volunteers
N/A
Genders Eligible for Study
Female
Sampling Method
Non-Probability Sample
Study Population
women who have induced abortion in early pregnancy (<12 weeks of gestation)
Description
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 Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
adverse pregnancy outcomes
Time Frame: 2021.6
|
the rate of different adverse pregnancy outcomes
|
2021.6
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Complications
Time Frame: 2020.6
|
the rate of different complications
|
2020.6
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Pei Kaiyan, National Research Institute for Family Planning (NRIFP)
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
June 1, 2019
Primary Completion (Anticipated)
June 1, 2020
Study Completion (Anticipated)
June 1, 2022
Study Registration Dates
First Submitted
November 28, 2019
First Submitted That Met QC Criteria
November 28, 2019
First Posted (Actual)
December 3, 2019
Study Record Updates
Last Update Posted (Actual)
December 3, 2019
Last Update Submitted That Met QC Criteria
November 28, 2019
Last Verified
June 1, 2019
More Information
Terms related to this study
Other Study ID Numbers
- No.2018-I2M-1-004
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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