erve block for pain relief in in patients operated for fracture femur neck
Not Applicable
- Conditions
- Health Condition 1: S720- Fracture of head and neck of femur
- Registration Number
- CTRI/2020/01/022681
- Lead Sponsor
- Dr S N medical collage and attached hospital Jodhpur
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Patients aged 18 to 70 years of either sex, ASA physical statue I and II undergoing fracture femur surgery who willing to participate in the study.
Exclusion Criteria
Patient refusal, hypersensitivity to amide local anaesthetics, infection at the injection site, pregnant woman, obesity, uncooperative patients, anatomical abnormality, bleeding disorders, peripheral neuropathy or neurological deficit, concurrent chronic analgesic therapy, known hepatic or renal insufficiency.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Duration of analgesiaTimepoint: upto 24 hours after surgery
- Secondary Outcome Measures
Name Time Method Onset and duration of sensory block <br/ ><br>Onset and duration of motor block <br/ ><br>To assess quality of analgesia while positioning the patient during the spinal anaesthesia <br/ ><br>Haemodynamic parameters (heart rate, blood pressure, SpO2) <br/ ><br>Any side effects of drugs <br/ ><br>Adequacy of block <br/ ><br>Patient satisfaction <br/ ><br>Timepoint: upto 24 hours after surgery