Cesarean Scar Pregnancy and Clinical Outcomes
Launched by PEKING UNIVERSITY THIRD HOSPITAL · Jul 28, 2022
Trial Information
Current as of June 26, 2025
Not yet recruiting
Keywords
ClinConnect Summary
This clinical trial, led by Professor Zhao Yangyu at Peking University Third Hospital, is looking at a specific condition called cesarean scar pregnancy. This happens when a pregnancy grows in the scar tissue from a previous cesarean section (C-section). The study aims to understand the risks and outcomes for women with this condition, including potential issues like blood loss, the need for additional surgeries, or the risk of miscarriage.
To participate in this trial, women must be at least 20 years old, have been diagnosed with a cesarean scar pregnancy, and be less than 14 weeks pregnant. They should also plan to receive care and give birth at the study hospital. Women who cannot give informed consent or have mental health disorders will not be eligible. If you qualify, you can expect to receive prenatal care and be closely monitored throughout your pregnancy as part of the study. This research could help improve care for future patients facing similar challenges.
Gender
FEMALE
Eligibility criteria
- 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
About Peking University Third Hospital
Peking University Third Hospital is a leading medical institution in China, renowned for its commitment to advanced healthcare, innovative research, and comprehensive clinical services. As a prominent sponsor of clinical trials, the hospital emphasizes the integration of cutting-edge scientific research with patient-centered care to enhance therapeutic outcomes. With a multidisciplinary approach, the institution fosters collaboration among top-tier medical professionals and researchers, striving to contribute to the global medical community through rigorous clinical studies that address pressing health challenges. Its dedication to ethical standards and regulatory compliance ensures the safety and efficacy of new treatments, ultimately aiming to improve patient care and outcomes on both a national and international scale.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Patients applied
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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