Ignite Creation Date:
2024-05-11 @ 8:30 AM
Last Modification Date:
2024-10-26 @ 3:28 PM
Study NCT ID:
NCT06402006
Status:
RECRUITING
Last Update Posted:
2024-05-08
First Post:
2024-04-28
Brief Title:
A Comparative Study Between Ultrasound Guided Erector Spinae Plane Block and Combined Ultrasound Guided Pericapsular Nerve Group and Lateral Femoral Nerve Block Following Total Hip Arthroplasty
Sponsor:
Ain Shams University
Organization:
Ain Shams University
Study Overview
Official Title:
A Comparative Study Between Ultrasound Guided Erector Spinae Plane Block and Combined Ultrasound Guided Pericapsular Nerve Group PENG and Lateral Femoral Nerve Block Following Total Hip Arthroplasty
Status:
RECRUITING
Status Verified Date:
2024-08
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief 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 002mgkg with or without fentanyl 05-1 mcgkg 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
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 002mgkg with or without fentanyl 05-1 mcgkg 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
Detailed Description:
None
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None