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

Recruiting Observational Study
Fibroid Uterus Polyp Uterus Retained Products of Conception
No Placebo Group Every participant receives an active treatment — no one gets a placebo. No Study Drug Researchers observe your health over time — no experimental treatment is given.
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At a Glance
Age
18 and older
Sex
Female
Study type
Observational
Participants needed
400 (estimated)
Sponsor
Centre Hospitalier Intercommunal Creteil · Other
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About This Trial
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…
Trial Locations
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Eligibility Criteria
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
Contacts

Yann SALHI, MD

0157022000

yann.salhi@chicreteil.fr

CONTACT

Elie MOSNINO, MD

elie.mosnino@gmail.com

CONTACT