Identifying outcomes of robotic surgery for uterine fibroids
Clinical Outcomes of Robotic Myomectomy: Comparisons of Without Versus With Temporary or Permanent Uterine Artery Occlusion.
This study is trying to find out what factors affect recovery and results for women having robotic surgery to remove uterine fibroids.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 400 (estimated) |
| Ages | 20 Years and up |
| Sex | Female |
| Sponsor | Far Eastern Memorial Hospital Academic / other |
| Locations | 1 site (Banqiao, New Taipei) |
| Trial ID | NCT06208891 on ClinicalTrials.gov |
What this trial studies
This study aims to identify the predictors of perioperative outcomes in women undergoing robotic myomectomy for uterine myoma, the most common gynecological tumor. It focuses on analyzing various factors that may influence surgical results and recovery in this patient population. By observing women who have received robotic myomectomy, the study seeks to gather data that could enhance surgical practices and patient care in the future.
Who should consider this trial
Good fit: Ideal candidates for this study are women over 20 years old who have undergone robotic myomectomy.
Not a fit: Patients who have not received robotic myomectomy or are under 20 years old may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could improve surgical outcomes and recovery for women undergoing robotic myomectomy.
How similar studies have performed: While there have been studies on surgical outcomes for myomectomy, this specific focus on robotic myomectomy and its predictors is relatively novel.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion criteria * \>20 years old women * women who received robotic myomectomy
Where this trial is running
Banqiao, New Taipei
- Department of Obstetrics and Gynecology, Far Eastern Memorial Hospital — Banqiao, New Taipei, Taiwan (Recruiting)
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.