Postoperative Pain Management with Continuous Wound Infiltration in Patients undergoing Posterior Spinal Fusion for Adolescent Idiopathic Scoliosis
Not Applicable
- Conditions
- Adolescent idiopathic scoliosis
- Registration Number
- JPRN-UMIN000029865
- Lead Sponsor
- Keio University School of Medicine
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 40
Inclusion Criteria
Not provided
Exclusion Criteria
Patients who are contraindicated to any study medications, who cannot answer the questionnaire and patients that the physician deems inappropriate.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Cumulative morphine consumption within 48h after surgery.
- Secondary Outcome Measures
Name Time Method Pain scores (Numerical Rating Scale, 0-10), sedation scales, incidence of postoperative nausea and vomiting, antiemetic consumption and incidence of pruritus in the 48h after surgery.