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Clinical Outcomes of Robotic Myomectomy

Clinical Outcomes of Robotic Myomectomy: Comparisons of Without Versus With Temporary or Permanent Uterine Artery Occlusion.

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06208891
Enrollment
400
Registered
2024-01-17
Start date
2023-11-21
Completion date
2024-12-31
Last updated
2024-01-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Women With Uterine Myoma

Brief summary

To identify the predictors of perioperative outcomes in women who receive robotic myomectomy

Detailed description

Uterine myoma is the most common gynecological tumor. Current surgical management was inclusive of conventional abdominal myomectomy, laparoscopy-assisted myomectomy, robotic-assisted myomectomy. The aim of this study was to identify the predictors of perioperative outcomes in women who receive robotic myomectomy

Interventions

PROCEDURERobotic myomectomy

Robotic assisted laparoscopic myomectomy

Sponsors

Far Eastern Memorial Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
20 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* \>20 years old women * women who received robotic myomectomy

Design outcomes

Primary

MeasureTime frameDescription
Surgical time1 weekFactors (e.g., the location and largest diameter of the uterine myoma) predicting surgical time

Secondary

MeasureTime frameDescription
Intraoperative blood loss1 weekFactors (e.g., the location and largest diameter of the uterine myoma) predicting intraoperative blood loss

Countries

Taiwan

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026