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Clinical Trials in France / NCT07146659
Recruiting Observational

Comparison of Operative Hysteroscopy Performed in the Operating Room Versus Outpatient Settings

NCT07146659 · tracked via the Priya Life Science France tracker
Sponsor
Centre Hospitalier Intercommunal Creteil
Phase
Observational
Started
2025-07-01
Last updated
2025-08-28

Condition(s) studied

Fibroid UterusPolyp UterusRetained Products of Conception

Study summary

This is an observational prospective monocentric study which aims to compare operative hysteroscopies performed in the operating room under general or loco-regional anesthesia and those performed outside the operating room (outpatient operative hysteroscopy). The primary outcome is the success rate of the procedure. Secondary outcomes include postoperative pain, patient satisfaction, complications, and time to return to work.

Eligibility

Sex
FEMALE
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Women aged ≥ 18 years -⁃ Undergoing operative hysteroscopy for intrauterine pathology * Able to provid e informed non-opposition * French-speaking Exclusion Criteria: * Patients with contraindications to hysteroscopy * Pregnancy * Inability to complete follow-up

Primary outcome measure(s)

  • This will be assessed as an ordinal qualitative variable, with procedures classified into three categories:number of complete success, number of partial success, or number of failure. — The classification will be determined by the surgeon at the end of the procedure and documented in the operative report (baseline)

Trial sites (1)

FacilityCityRegionStatus
CHI Créteil - Gynécologie et obstétrique Créteil France Recruiting

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Other trials for the same condition

Diagnostic Performances of Preoperative Echo-guided Uterine Biopsy in the Management of Suspect Uterine Sarcoma Tumors (BIOPSAR) Active, not recruiting
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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07146659 on ClinicalTrials.gov ↗ ← All trials in France