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Recruiting NCT07146659

NCT07146659 Comparison of Operative Hysteroscopy Performed in the Operating Room Versus Outpatient Settings

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Clinical Trial Summary
NCT ID NCT07146659
Status Recruiting
Phase
Sponsor Centre Hospitalier Intercommunal Creteil
Condition Fibroid Uterus
Study Type OBSERVATIONAL
Enrollment 400 participants
Start Date 2025-07-01
Primary Completion 2027-05-31

Eligibility & Interventions

Sex Female only
Min Age 18 Years
Max Age N/A
Study Type OBSERVATIONAL

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.

This trial targets 400 participants in total. It began in 2025-07-01 with a primary completion date of 2027-05-31.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief 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 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

Contact & Investigator

Central Contact

Yann SALHI, MD

✉ yann.salhi@chicreteil.fr

📞 0157022000

Frequently Asked Questions

Who can join the NCT07146659 clinical trial?

This trial is open to female participants only, aged 18 Years or older, studying Fibroid Uterus. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07146659 currently recruiting?

Yes, NCT07146659 is actively recruiting participants. Contact the research team at yann.salhi@chicreteil.fr for enrollment information.

Where is the NCT07146659 trial being conducted?

This trial is being conducted at Créteil, France.

Who is sponsoring the NCT07146659 clinical trial?

NCT07146659 is sponsored by Centre Hospitalier Intercommunal Creteil. The trial plans to enroll 400 participants.

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