Recruiting NCT04183829
Effects of Prior Induced Termination of Pregnancy on Complications and Pregnancy Outcomes.
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: induced termination of pregnancy.
- Who it may be relevant to
- Registry conditions: Reproductive Health, Abortion. Basic parameters: 18 years — 40 years · Female.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- China
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Overview
A prospective multicenter cohort study to evaluate effects of prior induced termination of pregnancy on complications and pregnancy outcomes.
Detailed description
A prospective multicenter cohort study to evaluate effects of prior induced termination of pregnancy on complications and pregnancy outcomes.
Interventions
- 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.
Primary outcome measures
- adverse pregnancy outcomes [Time frame: 2028.6]
Secondary outcome measures (1)
- Complications [Time frame: 2020.6]
Eligibility criteria
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
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Study design
- Observational model
- Cohort
Study locations
China · 12 centers
- Zhongshan Boai Hospital — Zhongshan
- Zhangjiakou Maternal and Child Health Hospital — Zhangjiakou
- Daqing People's Hospital — Daqing
- Changzhou Maternal and Child Health Hospital — Changzhou
- Yangzhou Maternal and Child Health Hospital — Yangzhou
- People's Hospital of Inner Mongolia Autonomous Region — Hohhot
- Qingdao Maternal and Child Health Hospital — Qingdao
- Zaozhuang Maternal and Child Health Hospital — Zaozhuang
- … and 4 more centers
Identifiers
NCT: NCT04183829 · No.2018-I2M-1-004