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Clinical Trials/NL-OMON26448
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.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
2 years ago
Study Type
Interventional

Investigators

Sponsor
Máxima Medisch Centrum, Veldhoven

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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