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Comparison of Robot-assisted Laparoscopic Myomectomy With Traditional Laparoscopic Myomectomy

Sponsor
Far Eastern Memorial Hospital (Other)
Overall Status
Completed
CT.gov ID
NCT01542658
Collaborator
(none)
42
Enrollment
1
Location

Study Details

Study Description

Brief Summary

This study is to reveal any potential advantage of Robot-assisted Laparoscopic Myomectomy (RLAM) over Traditional Laparoscopic Myomectomy (TLM) by comparing the perioperative variables and short-term outcome of RALM and TLM patients.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    All patients with symptomatic uterine myomas who underwent traditional laparoscopic myomectomy or robotic laparoscopic myomectomy were enrolled.

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    42 participants
    Observational Model:
    Case-Control
    Time Perspective:
    Retrospective
    Study Start Date :
    Feb 1, 2012
    Actual Primary Completion Date :
    Feb 1, 2012
    Actual Study Completion Date :
    Feb 1, 2012

    Arms and Interventions

    Arm Intervention/Treatment
    uterine myoma

    Outcome Measures

    Primary Outcome Measures

    1. amount of postoperation abdominal drainage [5 days]

    Secondary Outcome Measures

    1. operation time [1 day]

    2. blood loss [1 day]

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    20 Years and Older
    Sexes Eligible for Study:
    Female
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • cases with uterine myoma

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Department of Obstetrics and Gynecology, Far-Eastern Memorial Hospital Banqiao New Taipei Taiwan 22050

    Sponsors and Collaborators

    • Far Eastern Memorial Hospital

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Sheng-Mou Hsiao, Chief, Department of Obstetrics & Gynecology, Far Eastern Memorial Hospital
    ClinicalTrials.gov Identifier:
    NCT01542658
    Other Study ID Numbers:
    • 100167-E
    First Posted:
    Mar 2, 2012
    Last Update Posted:
    Mar 2, 2012
    Last Verified:
    Feb 1, 2012
    Additional relevant MeSH terms:
    Leiomyoma
    Myofibroma

    Study Results

    No Results Posted as of Mar 2, 2012