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Clinical Trial Summary

The patients will be randomized into 2 equal groups by a computer-generated random numbers table, named group A, B. Group A: patients will receive Pericapsular nerve group block and lateral femoral cutaneous nerve blocks. Group B: Patients will receive Erector spinae plane block block. After IV access insertion and oxygen nasal cannula application, monitoring will be applied for all patients, sedation in the form of midazolam 0.02mg/kg with or without fentanyl 0.5-1 mcg/kg will be administered to any of the patients who felt discomfort or could not tolerate the procedure. For (Group B) PENG block will be done before spinal anesthesia. LFCN block will be performed. For (Group A), ESP block will be done before spinal anesthesia. Spinal anesthesia will be chosen as the main anesthetic technique. In postoperative period all patients will receive the same adjuvant multimodal analgesia which will be 1000 mg of paracetamol with or without 30 mg ketorolac depending on comorbidities and depending on the patients" needs.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT06402006
Study type Interventional
Source Ain Shams University
Contact Riham Fa Galal, MD
Phone 01022739211
Email rihamfathygalal@gmail.com
Status Not yet recruiting
Phase N/A
Start date May 2024
Completion date November 2024

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