Pericapsular Nerve Block Versus Propofol During Hip Fractures Surgery
Not Applicable
Not yet recruiting
- Conditions
- Difference in Reduction in Visual Analogue Score at 30 Minutes
- Interventions
- Procedure: pericapsular nerve group block for group A,low dose intravenous Propofol [0.7mg/kg] over 30 seconds for group B
- Registration Number
- NCT06631118
- Lead Sponsor
- Ain Shams University
- Brief Summary
The study will compare the efficacy of Pericapsular nerve group block (PENG) versus low dose Propofol for the achievement of painless sitting position before spinal anesthesia in patients undergoing repair of Hip fractures.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- NOT_YET_RECRUITING
- Sex
- All
- Target Recruitment
- 60
Inclusion Criteria
- All patients in the age group ranging 40-70, both genders, belonging to physical status American Society of Anaesthesiologists (ASA) I and II
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Exclusion Criteria
- Patients with old fractures (more than 7 days), polytrauma, bleeding disorders or coagulopathy, local site infection, difficulty expressing pain scores such as hearing disability, mentally challenged, dementia or psychiatric illness and who refused to take part
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Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Group A pericapsular nerve group block for group A,low dose intravenous Propofol [0.7mg/kg] over 30 seconds for group B Group (A ) : will receive ultrasound guided pericapsular nerve group block (PENG) followed by spinal anesthesia. Group B pericapsular nerve group block for group A,low dose intravenous Propofol [0.7mg/kg] over 30 seconds for group B Group B will receive low dose intravenous Propofol \[0.7mg/kg\] over 30 seconds followed by spinal anesthesia and so far, this is the most common and standard technique to achieve sitting position during spinal anesthesia for patients with hip fractures.
- Primary Outcome Measures
Name Time Method The difference in VAS scale 30 min after giving propofol and the PENG block. The primary outcome will be difference in median reduction in VAS-D .
- Secondary Outcome Measures
Name Time Method