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Clinical Trials/NCT05652075
NCT05652075
Recruiting
Not Applicable

Efficacy and Safety of Ultrasound Guided Combined Pericapsular Nerve Group Block and Lateral Femoral Cutaneous Nerve Versus Lumbar Plexus Block for Postoperative Analgesia After Total Hip Arthroplasty: Randomized Clinical Study.

Minia University1 site in 1 country66 target enrollmentJanuary 1, 2023
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ConditionsPost Operative PainRegional Block

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Post Operative Pain
Sponsor
Minia University
Enrollment
66
Locations
1
Primary Endpoint
Visual analogue scale pain scores
Status
Recruiting
Last Updated
2 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSitesSimilar Trials

Overview

Brief 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.

Registry
clinicaltrials.gov
Start Date
January 1, 2023
End Date
February 1, 2024
Last Updated
2 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Minia University
Responsible Party
Principal Investigator
Principal Investigator

Hassan Mokhtar Elshorbagy Hetta

lecturer of anesthesia and ICU

Minia University

Eligibility Criteria

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.

Outcomes

Primary Outcomes

Visual analogue scale pain scores

Time Frame: 24 hour

pain score from 0-10 which 0 mean no pain and 10 the worst pain

Secondary Outcomes

  • first analgesic request(24 hour)
  • total analgesic consumption(24 hour)
  • First time to ambulate(24 hours)

Study Sites (1)

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