Consideration of preventing effect for postoperative pain and nausea and vomiting by perioperative suppot center.
Not Applicable
Completed
- Conditions
- Scheduled gynecologic surgical patients assisted by laparoscopic surgery
- Registration Number
- JPRN-jRCT1090220326
- Lead Sponsor
- TERUMO CORPORATIO
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- Female
- Target Recruitment
- 200
Inclusion Criteria
The inclusion criteria were patients aged 20 years or older women who were classified as class I or II by the American Society of Anesthesiologists Physical Status (ASA-PS) scale.
Exclusion Criteria
The exclusion criteria were as follows: patients with liver dysfunction (AST or ALT > 100U/L) u/L, medicine antienemics before surgery,and/or difficulty walking before surgery.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The primary aim of this study is to assess the effect of perioperative suppot center on recovery after surgery in patients undergoing laparoscopic gynecologic surgery following our hospital's management<br>protocol. The primary outcome is the rate of drinking,eating and mobilizing(out of bed).
- Secondary Outcome Measures
Name Time Method The second aim of this study was to assess the economic burden and effect of scheduled intravenous acetaminophen<br>(SIVA) on the analgesic activity in patients undergoing laparoscopic gynecologic surgery following our hospital's management<br>protocol.