Status:
COMPLETED
Hyaluronic Acid and Uterine Synechiae
Lead Sponsor:
Assistance Publique - Hôpitaux de Paris
Conditions:
Uterine Synechiae After Scraping for Natural Miscarriage
Eligibility:
FEMALE
18-46 years
Phase:
PHASE3
Brief Summary
The primary purpose of the study is to compare efficiency of a non-stick gel application after scraping surgery for natural miscarriage with no non-stick gel application after scraping surgery. Post-...
Detailed Description
Women patients coming for natural miscarriage will be compared according to whether a non-stick gel will be applicated or not after scraping surgery. 6-8 weeks after this surgery uterine synechiae ra...
Eligibility Criteria
Inclusion
- Women patients aged between 18 and 46 years old
- Term ≥ 7 weeks amenorrhea and ≤ 14 weeks amenorrhea
- Blighted ovum or not completed miscarriage or haemorrhagic miscarriage or retention miscarriage
- Consent signature
- Social security coverage
- Women who wants to be pregnant
Exclusion
- Infected miscarriage
- Uncertain diagnosis between miscarriage and extra-uterine pregnancy
- Hydatiform mole
- Uterine synechiae history
- Surgical zone infection
- Hyalobarrier® gel Endo hypersensitivity
- Clotting disorder
- Unstable diabetes
- Maternal malignant diseases
- Psychiatric disorder
- Incapacity in understanding the consent form and the questionnaires
- Law protected adult person
Key Trial Info
Start Date :
November 14 2014
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
September 14 2018
Estimated Enrollment :
364 Patients enrolled
Trial Details
Trial ID
NCT02248376
Start Date
November 14 2014
End Date
September 14 2018
Last Update
August 3 2021
Active Locations (1)
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1
Hôpital Lariboisière - Service de Gynécologie-Obstétrique
Paris, France, 75010