NL-OMON26448
Not yet recruiting
Not Applicable
A randomized controlled trial comparing paracervical block with a combination of paracervical block and fundal anesthesia during endometrial ablation in the outpatient clinic.
Máxima Medisch Centrum, Veldhoven0 sites96 target enrollmentTBD
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Endometrial ablationNovasureLocal anesthesiaParacervical blockFundal blockEndometriumablatieNovasureLokale anesthesieParacervicaal blockFundusblokkade
- Sponsor
- Máxima Medisch Centrum, Veldhoven
- Enrollment
- 96
- Status
- Not yet recruiting
- Last Updated
- 2 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Premenopausal women (≥18 years), ASA classification 1\-2, with menorrhagia, who are planned for a NovaSure endometrial ablation under local anesthesia.
Exclusion Criteria
- •Women younger than 18 years
- •Women who do not understand Dutch
Outcomes
Primary Outcomes
Not specified
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