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Comparison of two anesthesia methods in patients to undergo partial hip prosthesis

Phase 4
Completed
Conditions
Regional anesthesia,partial hip prosthesis
Regional anesthesia,
partial hip prosthesis
Anaesthesiology - Anaesthetics
Musculoskeletal - 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
NameTimeMethod
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
NameTimeMethod
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.]
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