N/A
20 Years
70 Years
20 Years
70 Years
Not Enrolling
Female
Myoma of Uterus
Female
Myoma of Uterus
Trial Information
Inclusion Criteria:
- ASA class I or II
- age 20~70
- patients undergoing total laparoscopic hysterectomy
Exclusion Criteria:
- history of shoulder surgery
- coagulopathy
- infection or trauma of shoulder
- general inflammation
- allergy to local anesthetics
Type of Study:
Interventional
Study Design:
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Prevention
Outcome Measure:
postoperative shoulder pain
Outcome Description:
Postoperative shoulder pain is measured using the VAS at 3 hr after end of surgery.
Outcome Time Frame:
3 hr after end of surgery
Safety Issue:
No
Authority:
South Korea: Institutional Review Board
Study ID:
4-2013-0101
NCT ID:
NCT01845532
Start Date:
April 2013
Completion Date:
November 2013
Related Keywords:
- Myoma of Uterus
- Myoma
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