A study on the perioperative management after posterior spinal infusion - the effect of clinical pathway with around the clock analgesic medication.
Not Applicable
- Conditions
- Posterior spinal infusion
- Registration Number
- JPRN-UMIN000051149
- Lead Sponsor
- Saiseikai Yokohamashi Tobu Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 76
Inclusion Criteria
Not provided
Exclusion Criteria
(1)Elevation of liver enzyme in postoperative period. (2)Patients with alcoholic liver dysfunction. (3)Patients in post group not undergo patent support center. (4)Patients with unevaluable NRS and PONV. (5)Patients with posterior spinal infusion with anterior infusion or multiple vertebral bodies. (6)Patients with postoperative major complication.
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method RS point at rest in POD1
- Secondary Outcome Measures
Name Time Method RS point at rest from surgery end to POD3 The frequency of using analgesia. The frequency of using antiemetic. The day of getting out of bed. The score of getting out of bed. Amount of food eaten at first time meal.