Comparison of different doses of parecoxib for the prevention of postanesthetic shivering.
Not Applicable
Recruiting
- Conditions
- patients undergoing general anesthesia were recruited into the study
- Registration Number
- JPRN-UMIN000012624
- Lead Sponsor
- Department of Anaesthesiology, Southwest Hospital,
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 120
Inclusion Criteria
Not provided
Exclusion Criteria
1, initial body temperature more than 38 centigrade or less than 36.5 centigrade; 2, hyperthyroidism, hypertension, diabetes mellitus, impaired renal or liver functions, endocrine or cardiopulmonary disease; 3, taking vasoactive or antidepressant drugs, receiving intraoperative blood or blood products transfusion; 4, known history of alcohol or substance abuse, or possible pregnancy;
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method the overall incidence and grades of postoperative shivering
- Secondary Outcome Measures
Name Time Method