Patient Controlled Analgesia for Total Hip or Knee Arthroplasty
Phase 2
- Conditions
- post hip or knee arthroplasty surgery pain.Adjustment and management of infusion pump
- Registration Number
- IRCT138902023771N1
- Lead Sponsor
- Vice Chancellor for Research & Technology, Isfahan University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 60
Inclusion Criteria
Inclusion Criteria of the study :patients that are in the range of 40-80 years ,have 1-3 ASA ,are candidates of hip or knee replacement surgery & sign the consent form. Non inclusion criteria:patients that have contraindication for regional anesthesia or coagulopathy ,platelet count less than 100000 or chronic renal failure (G.F.R<60),and narcotic addiction . Exclusion criteria : Incomplete regional anesthesia, change to spinal anesthesia.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Postoperative pain. Timepoint: 0, 6, 12, and 24 hours after operation. Method of measurement: Visual analogue Scale.;Level of Conciousness. Timepoint: 0, 6, 12, and 24 hours after operation after recovery room enterance. Method of measurement: A 4 point likert scale.;Pulse rate. Timepoint: 0, 6, 12, and 24 hours after operation. Method of measurement: pulse oximeter.;Blood pressure. Timepoint: 0, 6, 12, and 24 hours after operation. Method of measurement: oscillometer.;Hypoxia. Timepoint: postoperative within 24 hours of surgery. Method of measurement: pulse oximeter.
- Secondary Outcome Measures
Name Time Method rinary retention. Timepoint: postoperative within 24 hours of surgery. Method of measurement: using checklist.;Pruritus. Timepoint: postoperative within 24 hours of surgery. Method of measurement: using checklist.;Vomitting and Nausea. Timepoint: postoperative within 24 hours of surgery. Method of measurement: using checklist.