Study comparing the pain reveling capacity of PENG block and femoral nerve block during positioning patients with hip fracture for spinal anesthesia
- Conditions
- Health Condition 1: O- Medical and Surgical
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 70
1) Patients belonging to ASA grade I, II and III with hip fractures, posted for surgery
under spinal anaesthesia who are unable to sit due to pain in the hip joint.
2) Patients of either sex, between the age group 21 to 80 years.
3) Patients who give a valid informed consent.
1) Patient not willing to participate in the study.
2) Patients belonging to ASA grade IV and above .
3) Patients with hip fractures who are able to sit comfortably without pain.
4) Patients with hemorrhagic diathesis, neurological disorders, psychiatric disorders.
5) Previous femoral bypass surgery.
6) Patients with allergy to local anaesthetics.
7) Patients with polytrauma, infection over the injection site.
8) Morbid obesity.
9) Patients with spinal deformities.
10) Patients with language barrier.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method THE STUDY WILL BE ABLE TO COMPARE THE REDUCTION IN VAS SCORE BETWEEN PENG BLOCK AND FEMORAL NERVE BLOCK AND TELL WHICH BLOCK IS BETTER IN REDUCING VAS SCORE WHILE POSITIONING PATIENTS FOR SPINAL ANAESTHESIATimepoint: VAS score will be assessed before block at rest and on straight leg raising. Post block at 15 minutes, 30 minute, 4 hours,6 hours, 12 hours and 24 hours.
- Secondary Outcome Measures
Name Time Method 1. To asses the sitting angle <br/ ><br>2. To assess the anaesthetist satisfaction score for performing spinal anaesthesia. <br/ ><br>3. To assess the additional dose of fentanyl for reduction of VAS less than 3 for positioning. <br/ ><br>4. To assessthe patientâ??s satisfaction Score. <br/ ><br>5. To assess the duration of analgesiaTimepoint: will be assessed 15 minutes post block