NCT06208891

Brief Summary

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

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
400

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Nov 2023

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

November 21, 2023

Completed
14 days until next milestone

First Submitted

Initial submission to the registry

December 5, 2023

Completed
1 month until next milestone

First Posted

Study publicly available on registry

January 17, 2024

Completed
12 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 31, 2024

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 31, 2024

Completed
Last Updated

January 17, 2024

Status Verified

December 1, 2023

Enrollment Period

1.1 years

First QC Date

December 5, 2023

Last Update Submit

January 5, 2024

Conditions

Women With Uterine Myoma

Outcome Measures

Primary Outcomes (1)

  • Surgical time

    Factors (e.g., the location and largest diameter of the uterine myoma) predicting surgical time

    1 week

Secondary Outcomes (1)

  • Intraoperative blood loss

    1 week

Study Arms (1)

Robotic myomectomy

Women who received robotic myomectomy

Procedure: Robotic myomectomy

Interventions

Robotic myomectomyPROCEDURE

Robotic assisted laparoscopic myomectomy

Robotic myomectomy

Eligibility Criteria

Age20 Years+
Sexfemale(Gender-based eligibility)
Gender Eligibility Detailswomen who received robotic myomectomy
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Women who received robotic-assisted myomectomy

You may qualify if:

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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Department of Obstetrics and Gynecology, Far Eastern Memorial Hospital

Banqiao District, New Taipei, 22050, Taiwan

RECRUITING

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
RETROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Chief, Department of Obstetrics & Gynecology

Study Record Dates

First Submitted

December 5, 2023

First Posted

January 17, 2024

Study Start

November 21, 2023

Primary Completion

December 31, 2024

Study Completion

December 31, 2024

Last Updated

January 17, 2024

Record last verified: 2023-12

Locations

TW(1)