UnknownNot Applicable

Cesarean Scar Pregnancy and Clinical Outcomes

500 participantsStarted 2022-08-01

Plain-language summary

This study is a prospective cohort study, led by Prof. Zhao Yangyu, from the Department of Gynecology \& Obstetrics, Peking University Third Hospital.

Who can participate

Age range20 Years – 49 Years

SexFEMALE

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Female aged ≥ 20 years * Female with cesarean scar pregnancy * Less than 14 gestational weeks * Planning to receive prenatal healthcare and delivery service at the study hospital Exclusion Criteria: * Inability to provide informed consent * Women with mental disorders

What they're measuring

Incidence of blood loss

Timeframe: delivery

Incidence of postpartum hemorrhage

Timeframe: delivery

Incidence of maternal transfusion

Timeframe: delivery

Incidence of spontaneous abortion

Timeframe: delivery

Incidence of stillbirth

Timeframe: delivery

Incidence of perinatal death

Timeframe: 42 days postpartum

Trial details

NCT IDNCT05481606

SponsorPeking University Third Hospital

Sponsor typeOTHER

Study typeOBSERVATIONAL

Primary completion2023-08-01

Contact for this trial

Yangyu Zhao, MD

13701118357 zhaoyangyu@bjmu.edu.cn

View on ClinicalTrials.gov More Blood Loss trials