Evaluation of the Endometrial Cavity After Endometrial Ablation

Stopped early · Not applicable

Conditions studied: Menorrhagia

In brief

The purpose of this study is to evaluate the shape, size and appearance of the inside of the uterus six months following an endometrial ablation procedure. Half of the participants will have their ablation performed with a hydrothermal ablation device and the other half will have their ablation performed with a device that uses radiofrequency energy.

Key facts

Study ID

NCT02087228

Run by

Baylor Research Institute

People needed

25

Starts

2013-09-01

Expected to finish

2015-07-01

Last updated by the study team

2016-01-18

Who can join

Age: 18 and older, up to 51. Sex: female. Healthy volunteers: not accepted.

You may qualify if…

• Premenopausal women Not pregnant and no future pregnancy desired Willing to randomize the device used for the ablation Willing to undergo diagnostic hysteroscopy with office-based anesthesia 6 months post-ablation

You may not qualify if…

• Pregnancy or desiring future pregnancy Endometrial hyperplasia Presence of active endometriosis Active pelvic inflammatory disease Previous endometrial ablation procedure

Where it is running

• Texas Health Care — Fort Worth, Texas, United States

Full record on ClinicalTrials.gov

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