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Fundal Block in Pre-menopausal Women to Reduce Pain During Outpatient-based Endometrial Ablation (FUNDAL-PAIN) — FUNDAL-PAIN  

Pain Clinical Trial

Official title:
FUndal Block During NovaSure enDometrial AbLation to Reduce Intraoperative PAIN: A Randomized Controlled Trial

Clinical Trial Summary

The objective of this study is to assess the efficacy of a fundal block in reducing women's perception of pain during NovaSure endometrial ablation (EA) in an outpatient-based setting.

Clinical Trial Description

The researchers aim to determine whether participants receiving the paracervical and fundal block (experimental group) achieve clinically and statistically significant reductions in self-reported pain during NovaSure EA, as compared to those receiving paracervical block (control group). All women will obtain concurrent procedural sedation. Women's perception of pain will be recorded on a scale from 0 to 10 using the visual analogue scale (VAS). The researchers hypothesize that the participants receiving combined paracervical and fundal block will experience less pain during the active procedure, as compared to those receiving paracervical block alone. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04249063
Study type Interventional
Source Saskatchewan Health Authority - Regina Area
Contact
Status Active, not recruiting
Phase N/A
Start date January 18, 2021
Completion date June 2023
View Details
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