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)

Enter a location and click search to find clinical trials sorted by distance.

Page 1 of 1 (1 locations)

1

Centre hospitalier intercommunal de poissy-saint germain en Laye

Poissy, France, 78300