CompletedPhase 3

Hyaluronic Acid and Uterine Synechiae

France364 participantsStarted 2014-11-14

Plain-language 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-scraping uterine synechiae rate will be established at the diagnostical hysteroscopy 6-8 weeks after surgery.

Who can participate

Age range18 Years – 46 Years

SexFEMALE

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * 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 Criteria: * 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

What they're measuring

Evaluation of post-surgical uterine synechiae rate during a diagnostical hysteroscopy.

Timeframe: 6-8 weeks after scraping surgery

Trial details

NCT IDNCT02248376

SponsorAssistance Publique - Hôpitaux de Paris

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2018-09-14

View on ClinicalTrials.gov More Uterine Synechiae After Scraping for Natural Miscarriage trials