Study of the Efficacy of a Novel Disposable Patient-Controlled Analgesia Device in Postoperative Pai
Not Applicable
- Conditions
- an upper abdominal surgery
- Registration Number
- JPRN-UMIN000006871
- Lead Sponsor
- Kawasaki Medical University Department of Anesthesiology & Intensive Care Medicine 2
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 60
Inclusion Criteria
Not provided
Exclusion Criteria
Patients who are considered ineligible for participation in the present study by the attending physician.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Wound pain level (resting and moving VAS) Number of requests for PCA and actual number of administrations Total local anesthetic dose Use of rescue drugs (drug, number of administrations and dose)
- Secondary Outcome Measures
Name Time Method Patient backgrounds such as age and sex, etc. Factors related to surgery, such as type, duration and bleeding volume etc. Insertion site and length, etc. in epidural anesthesia