Comparison of two anesthesia methods in patients to undergo partial hip prosthesis
Phase 4
Completed
- Conditions
- Regional anesthesia,partial hip prosthesisRegional anesthesia,partial hip prosthesisAnaesthesiology - AnaestheticsMusculoskeletal - Other muscular and skeletal disorders
- Registration Number
- ACTRN12613001186741
- Lead Sponsor
- Ayse Belin OZER
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- All
- Target Recruitment
- 50
Inclusion Criteria
planned to be operated by RA method and to undergo partial hip prosthesis
ASA III-IV
Exclusion Criteria
Patients that were allergic to local anesthesia, with neurological diseases, infection in the intervention area, with whom cooperation could not be established, and that did not accept the procedure were excluded from the study.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method anesthesia preparation time (from monitorized to beginning surgical procedure)[at anesthesia induction];Level of analgesia was evaluated with pinprick test[in 5-minute intervals following drug administration until appropriate sensorial levels was reached. ];motor block degree was assessed by modified Bromage scale (0: No block, 1: hip flexion blocked while knee is in extension, 2: Knee flexion blocked, 3: Complete motor block)[in 5-minute intervals following drug administration until a Bromage score of 2 or 3 (Complete motor block) was reached.]
- Secondary Outcome Measures
Name Time Method heart rate via electrocardigraphy[5-minute intervals from preoperative till the end of peroperative operation times];mean arterial pressure via noninvasive blood pressure measure (ossilometric)[5-minute intervals from preoperative till the end of peroperative operation times];peripheral oxygen saturation via pulse oximetry.[5-minute intervals from preoperative till the end of peroperative operation times];analgesic comsumption[24th hours postoperatively.]