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N/A
20 Years
N/A
Not Enrolling
Female
Uterine Myoma

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Trial Information


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


Inclusion Criteria:



- cases with uterine myoma

Type of Study:

Observational

Study Design:

Observational Model: Case Control, Time Perspective: Retrospective

Outcome Measure:

amount of postoperation abdominal drainage

Outcome Time Frame:

5 days

Safety Issue:

No

Authority:

Taiwan: Institutional Review Board

Study ID:

100167-E

NCT ID:

NCT01542658

Start Date:

February 2012

Completion Date:

February 2012

Related Keywords:

  • Uterine Myoma
  • Myoma
  • Leiomyoma
  • Myofibroma

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