Stopped: Data collection was not possible due to failure to maintain assigned uterine pressure from uncontrollable intraoperative fluctuations. Without stable pressure in either group, data would be invalid.
The aim of the study is to compare the outcomes of patients undergoing hysteroscopy with a MyoSure device with a pressure of 60 mmHg to those using the standard of 80 mmHg.
Age range
18 Years
Sex
FEMALE
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
Physician Survey to Assess Visualization
Timeframe: Through study completion, an average of 1 year
Procedure Time
Timeframe: Through study completion, an average of 1 year
Specimen Weight
Timeframe: Through study completion, an average of 1 year
Amount of Fluid
Timeframe: Through study completion, an average of 1 year
Lasix Administered Post-operatively
Timeframe: Through study completion, an average of 1 year
Change in Pressure Was Needed
Timeframe: Through study completion, an average of 1 year