20,000 women join study to uncover Abortion's impact on later pregnancies
NCT ID NCT04183829
First seen Jun 25, 2026 · Last updated Jun 26, 2026 · Updated 1 time
Summary
This study is following 20,000 women in China who had an induced abortion early in pregnancy (before 12 weeks). Researchers want to see if having an abortion in the past leads to more complications or problems in later pregnancies. The women will be tracked over time to compare their pregnancy outcomes with those who have not had a prior abortion. This is an observational study, meaning it only looks for patterns, not a treatment or cure.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If this study finds clear links, it could help doctors better counsel women about future pregnancy risks after an abortion.
- What could go wrong
- This is an observational study, not a treatment trial. It can show associations but not cause and effect, and results may take years to emerge.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 20,000 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jun 2019
- Expected to finish
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Jun 2028
An estimate. End dates often move.
- Lead sponsor
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A government agency
The lead sponsor is a government body.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
women who have induced abortion in early pregnancy (\<12 weeks of gestation)
- Ages
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18 to 40 years
- Sex
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Female participants only
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
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
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
10 sites. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Changzhou Maternal and Child Health Hospital
RECRUITINGChangzhou, Jiangsu, China
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Chongqing Health Center for Women and Children
RECRUITINGChongqing, China
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Daqing People's Hospital
RECRUITINGDaqing, Heilongjiang, 150000-160000, China
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People's Hospital of Inner Mongolia Autonomous Region
RECRUITINGHohhot, Mongolia Autonomous, China
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Qingdao Maternal and Child Health Hospital
COMPLETEDQingdao, Shandong, China
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Shenzhen Luohu Maternity and Child Healthcare Hospital
RECRUITINGShenzhen, China
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Taiyuan Maternal and Child Health Hospital
RECRUITINGTaiyuan, Shanxi, China
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Tanggu Maternal and Child Health Hospital
COMPLETEDTanggu, Tianjin Municipality, China
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Yangzhou Maternal and Child Health Hospital
RECRUITINGYangzhou, Jiangsu, China
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Zaozhuang Maternal and Child Health Hospital
RECRUITINGZaozhuang, Shandong, China
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Zhangjiakou Maternal and Child Health Hospital
RECRUITINGZhangjiakou, Hebei, China
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Zhongshan Boai Hospital
RECRUITINGZhongshan, Guangdong, China
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