CTRI/2024/04/065755
Not yet recruiting
Phase 3
Comparative Evaluation of Post-Operative Analgesic Efficacy of 15 ml of 0.375 % Ropivacaine versus 25 ml of 0.375 % Ropivacaine in patients undergoing hip fracture surgery under ultrasound guided Pericapsular Nerve Group Block: A Prospective Randomised Double Blinded Trial - NI
Aruna Bharti0 sites0 target enrollmentTBD
Overview
- Phase
- Phase 3
- Intervention
- Not specified
- Conditions
- Health Condition 1: S720- Fracture of head and neck of femurHealth Condition 2: S00-T88- Injury, poisoning and certain other consequences of external causes
- Sponsor
- Aruna Bharti
- Status
- Not yet recruiting
- Last Updated
- 2 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •1\.Patient who had given written informed consent
- •2\.Patients belonging to ASA grade I and II.
- •3\.All genders
- •4\.Patients in the age group of 18 yrs and above
- •5\.Patient with hip fracture ( fracture neck of femur, intertrochanteric and subtrochanteric fractures).
Exclusion Criteria
- •1\.Patient refusal.
- •2\.ASA grade III and IV
- •3\.Emergency surgeries
- •4\.Patients with polytrauma
- •5\.Patient who had allergy and intolerance to local anesthetics \& have active skin infection.
- •6\.Patient with cognitive impairment, delirium, dementia and severe hearing impairment
- •7\.Coexisting coagulopathy or anticoagulant or antiplatelet treatment that would be a contraindication to regional anesthesia.
- •8\.Patient having diabetes, ischemic and valvular heart disease, pre\-existing neurologic deficits in the limb .
Outcomes
Primary Outcomes
Not specified
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