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Failed Endometrial Ablation Treatment With Implantable Progesterone (FEAT) Study — FEATS  

Dysmenorrhea Clinical Trial

Official title:
Failed Endometrial Ablation Treatment With Implantable Progesterone (FEAT) Study

Clinical Trial Summary

The objective of this study is to assess the efficacy of an implantable etonogestrel device in reducing hysterectomy rate in patients with a failed endometrial ablation.

Clinical Trial Description

The researchers aim to determine whether use of etonogestrel implant in patients with failed endometrial ablation significantly decreases hysterectomy rate. Changes in pelvic pain and vaginal bleeding will be assessed. Time to hysterectomy will be examined. The researchers hypothesize that treatment of failed endometrial ablation with etonogestrel implant will decrease pelvic pain and vaginal bleeding resulting in a significantly decreased need for hysterectomy. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05227456
Study type Interventional
Source Saskatchewan Health Authority - Regina Area
Contact Sarah N Smith, MD
Phone 306-352-4963
Email SarahSmith@saskhealthauthority.ca
Status Recruiting
Phase Phase 2
Start date July 1, 2022
Completion date June 30, 2027
View Details
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