The Impact of Cesarean Scar Defects on the Success of Assisted Human Reproduction
Launched by UNIVERSITY HOSPITAL, ANGERS · Apr 27, 2021
Trial Information
Current as of July 26, 2025
Recruiting
Keywords
ClinConnect Summary
This clinical trial is looking at how a type of scar defect called an isthmocele—an abnormal thinning or weakening of the uterus wall where a previous cesarean section was done—might affect the success of assisted reproductive treatments like IVF (in vitro fertilization). The study focuses on women who have had at least one cesarean delivery, are experiencing difficulty getting pregnant again (secondary infertility), and are planning to use fertility treatments. Doctors use a special ultrasound test called hysterosonography to spot these scar defects before treatment.
Women between 18 and 43 years old who speak French, have had a cesarean section, and are preparing for IVF or similar procedures may be eligible to join. Participants will undergo the usual fertility assessments, including the hysterosonography to check for scar defects, and their fertility treatment outcomes will be monitored. The goal is to understand whether these uterine scars affect the chances of getting pregnant with assisted reproduction. This information could help guide future treatment decisions, such as whether surgery to repair the scar might improve fertility outcomes.
Gender
FEMALE
Eligibility criteria
- Inclusion criteria :
- • Patients with a history of at least one cesarean section (single or multi-scarred uterus).
- • Age between 18 and 43 years old
- • Secondary infertility requiring ART techniques (FIV or FIV ICSI).
- • A Hysterosonography examination as part of the pre-ART assessment allowing for the detection of the presence of an isthmocele.
- • French speaking patients
- • Patient affiliated to or beneficiary of a social security scheme
- Non-inclusion criteria :
- • - Refusal to participate in the study.
About University Hospital, Angers
The University Hospital of Angers is a leading academic medical institution dedicated to advancing healthcare through innovative research and clinical trials. As a prominent sponsor of clinical studies, the hospital leverages its multidisciplinary expertise and state-of-the-art facilities to investigate new therapeutic approaches and improve patient outcomes. Committed to excellence in patient care and medical education, the University Hospital of Angers collaborates with a network of researchers and healthcare professionals to facilitate groundbreaking studies across various medical fields, ensuring rigorous adherence to ethical standards and regulatory compliance. Through its clinical trial initiatives, the institution aims to contribute significantly to the advancement of medical knowledge and the development of effective treatments.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Angers, , France
Brest, , France
Rennes, , France
Saint étienne, , France
Nîmes, , France
Corbeil Essonnes, , France
Créteil, , France
Paris, , France
Rennes, , France
Patients applied
Trial Officials
Guillaume LEGENDRE, MD PhD
Principal Investigator
UH Angers
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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