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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05652075
Other study ID # 473:10/2022
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date January 1, 2023
Est. completion date February 1, 2024

Study information

Verified date October 2023
Source Minia University
Contact hassan m. hetta, lecturer
Phone 1010901114
Email hassan.hetta@mu.edu.eg
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Regional anesthesia for postoperative analgesia in THA includes epidural anesthesia and peripheral nerve blocks. However epidural anesthesia has a great role in THA, it has become restricted as perioperative antithrombotic drugs are generally used for orthopedic patients. the study aim to evaluate and compare efficacy and safety of pericapsular nerve group block (PENG) block and lateral femoral cutaneous nerve versus Lumbar plexus block on postoperative analgesia in hip surgery.


Recruitment information / eligibility

Status Recruiting
Enrollment 66
Est. completion date February 1, 2024
Est. primary completion date January 1, 2024
Accepts healthy volunteers No
Gender All
Age group 30 Years to 70 Years
Eligibility Inclusion Criteria: (ASA) physical status I to III scheduled for hip surgery aged (30-70) years Exclusion Criteria: - Drug allergy, - Morbid obesity (BMI >40 kg/m2), - Coagulopathy, - Psychiatric disorder, - Opioid dependence, - Patient refusal to give informed consent.

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
pericapsular nerve group and lateral femoral cutaneous nerve block
Will undergo pericapsular nerve group block (PENG) combined with lateral femoral cutaneous nerve under ultrasound guided block with 20 mL of 0.25% bupivacaine.
lumbar plexus block
Will undergo Lumbar plexus block (LPB) under ultrasound guided block with 20 mL of 0.25 % bupivacaine.

Locations

Country Name City State
Egypt Minia University Minya Minia

Sponsors (1)

Lead Sponsor Collaborator
Minia University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary Visual analogue scale pain scores pain score from 0-10 which 0 mean no pain and 10 the worst pain 24 hour
Secondary first analgesic request time to demand nalbuphine 24 hour
Secondary total analgesic consumption total nalbuphine in mg consumed in the first day 24 hour
Secondary First time to ambulate first time to move 24 hours
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