Status:
COMPLETED
Effectiveness of Hysteroscopy in the Treatment of Intrauterine Trophoblastic Retentions
Lead Sponsor:
Assistance Publique - Hôpitaux de Paris
Collaborating Sponsors:
URC-CIC Paris Descartes Necker Cochin
Conditions:
Incomplete Miscarriage
Eligibility:
FEMALE
18-44 years
Phase:
NA
Brief Summary
The purpose of this study of is to compare subsequent fertility rates between hysteroscopy and aspirative curettage in the surgical treatment of incomplete spontaneous abortion
Detailed Description
Incomplete spontaneous abortion (ISA) is defined by the intrauterine retention of conceptual product after incomplete or partial expulsion of the conceptual product. Treatment such retention may be ex...
Eligibility Criteria
Inclusion
- Major, under 45 years with intrauterine trophoblastic retention after incomplete miscarriage in the first quarter (termination of pregnancy \< 14 WA),
- With desire of pregnancy ;
- Intrauterine trophoblastic retention diagnosed by transvaginal pelvic ultrasound finding a intrauterine heterogeneous image or intrauterine gestational sac more than 15 mm in thickness, complicated or not of endometritis ;
- Decision to surgical management of incomplete miscarriage by the health care team ;
- Patient beneficiary or affiliated to a health insurance
- Informed and signed consent
Exclusion
- Will not be included in the protocol patients :
- having a uterine malformation known ;
- having received surgical treatment for the current intrauterine retention ;
- with intrauterine retention diagnosed by transvaginal pelvic ultrasound of more than 50 mm in thickness ;
- requiring a haemostatic act in urgency for heavy vaginal bleeding (miscarriage haemorrhage) ;
- bearer of intrauterine device ;
- having an evolutive pregnancy;
- having an ectopic pregnancy;
- having a trophoblastic retention following a voluntary abortion ;
- having a pregnancy achieved by medically assisted procreation
Key Trial Info
Start Date :
November 5 2014
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
July 3 2020
Estimated Enrollment :
577 Patients enrolled
Trial Details
Trial ID
NCT02201732
Start Date
November 5 2014
End Date
July 3 2020
Last Update
September 5 2025
Active Locations (1)
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1
Centre hospitalier intercommunal de poissy-saint germain en Laye
Poissy, France, 78300