to compare two methods of pain relief in elderly patients undergoing proximal femoral nailing
Not Applicable
- Conditions
- Health Condition 1: M00-M99- Diseases of the musculoskeletal system and connective tissue
- Registration Number
- CTRI/2023/01/048902
- Lead Sponsor
- Sancheti Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1. Age > 80 years
2. ASA I-III
3. Proximal femur fracture
4.Undergoing for femur nailing under spinal anesthesia
Exclusion Criteria
1. Any contraindication for spinal anaesthesia
2. intraoperative need for general anaesthesia
3.Not willing or unable to consent or cooperate for the block procedure
4.Mental disability or Inability to understand pain score
5. Any hemodynamic instability or respiratory compromise requiring vasopressors or oxygen therapy at the completion of surgery.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To assess postoperative pain scoresTimepoint: To assess postoperative pain scores at time 0, 4 hrs, 8 hrs, 12hr and 24 hrs
- Secondary Outcome Measures
Name Time Method 1.ultrasound visibility of the structures <br/ ><br>2. ICU length of stay <br/ ><br>3.the total duration of hospitalization <br/ ><br>4. incidence of rescue analgesia <br/ ><br>5. postoperative mobilisation <br/ ><br>6. cardiorespiratory and neurological events prior to discharge.Timepoint: 1. during the block <br/ ><br>2 and 3. at the time of ICU stay and discharge <br/ ><br>4. at 24 hrs <br/ ><br>5. after surgery <br/ ><br>6.postoperative period after surgery <br/ ><br>