Menorrhagia Clinical Trial
Official title:
Evaluation of the Endometrial Cavity After Endometrial Ablation
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.
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. Participants
are randomly assigned to one or the other device.
A vaginal ultrasound will be performed before the procedure and again at six months
post-procedure.
The inside of the uterus will be visualized via hysteroscopy before the procedure and again
at six months post-procedure. Measurements will be taken and the investigator will compare
photos taken pre-procedure and six months post-procedure.
;
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
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