To study the effect of two regional anesthesia techniques for adequate pain control after surgeries around hip joint
Not Applicable
Completed
- Conditions
- Health Condition 1: M169- Osteoarthritis of hip, unspecified
- Registration Number
- CTRI/2021/09/036787
- Lead Sponsor
- AIIMS Jodhpur
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 58
Inclusion Criteria
Belonging to American Society of Anesthesiologists Physical Status 1-3 and Scheduled for elective unilateral total hip replacement surgery.
Exclusion Criteria
1.Known hypersensitivity to any of the drugs used in the study.
2. Patient having infection at the site of block.
3. Patients with coagulopathy or on anticoagulation therapy.
4.Patients with untreated psychiatric illness.
5.Patients with known cardiac, hepatic or kidney diseases.
6.Opioid Dependency
7.Pre-existing neurologic or anatomic deficits in the lower extremities
8.Prior surgery in the corresponding side of the inguinal or suprainguinal area
9.Chronic pain syndromes requiring opioid intake at home
10.Pregnancy
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Post-operative pain relief assessed by Numeric Rating Scale (NRS) at fixed time intervalTimepoint: First 24 postoperative hours
- Secondary Outcome Measures
Name Time Method 1. Motor Blockade at fixed time interval <br/ ><br>2. The time of first rescue analgesic requirement. <br/ ><br>3. Total amount of analgesia consumed during 24-hours. <br/ ><br>4. Duration to perform block. <br/ ><br>5. Patient’s satisfaction for the mode of analgesia. <br/ ><br>6. Periprocedural complication. <br/ ><br>Timepoint: First 24 postoperative hours