Pain Characteristics After Total Laparoscopic Hysterectomy
NCT ID: NCT01838382
Last Updated: 2014-01-14
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
50 participants
INTERVENTIONAL
2013-03-31
2013-09-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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NA
SINGLE_GROUP
TREATMENT
NONE
Study Groups
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laparoscopic hysterectomy group
female patients undergoing total laparoscopic hysterectomy.
classic LMA insertion
Classic LMA (cLMA) will be inserted when no response is obtained in the train-of-four stimulation. The fiberoptic view through the LMA, intraoperative complications of the cLMA, any complication during anesthesia emergence will be recorded. The device is examined and noted for the presence of visible blood.
Interventions
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classic LMA insertion
Classic LMA (cLMA) will be inserted when no response is obtained in the train-of-four stimulation. The fiberoptic view through the LMA, intraoperative complications of the cLMA, any complication during anesthesia emergence will be recorded. The device is examined and noted for the presence of visible blood.
Eligibility Criteria
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Inclusion Criteria
* age \>=20, \<= 80 years
* female
* patients undergoing elective total laparoscopic hysterectomy
Exclusion Criteria
* abnormal mental status
* drug abuse
* chronic alcoholism
* immunosuppressants or steroid user
20 Years
80 Years
FEMALE
No
Sponsors
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Yonsei University
OTHER
Responsible Party
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Locations
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Severance hospital
Seoul, Seoul, South Korea
Countries
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Other Identifiers
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4-2012-0871
Identifier Type: -
Identifier Source: org_study_id
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