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.
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