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Clinical Trials/NCT04698746
NCT04698746
Recruiting
Not Applicable

Pericapsular Nerve Group (PENG) Block Versus Intra-articular Injection for Hip Arthroscopy: A Randomized Trial

Bezmialem Vakif University1 site in 1 country72 target enrollmentJanuary 20, 2021

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Opioid Use
Sponsor
Bezmialem Vakif University
Enrollment
72
Locations
1
Primary Endpoint
Postoperative opioid consumption
Status
Recruiting
Last Updated
2 years ago

Overview

Brief Summary

Hip arthroscopy is a popular surgical method that is increasingly being used for both intraarticular and extraarticular hip surgeries. Postoperative acute pain is difficult to control in hip surgeries due to the complex nature of hip innervation and the large number of surgical interventions. Optimal treatment of postoperative pain in hip arthroscopy is very important to be able to perform rehabilitation, avoid opioid side effects and minimize unplanned re-hospitalization. Regional anesthesia techniques are widely used because of their proven efficacy in post-surgical pain management and their safety profile that ultimately contributes to early recovery. Many regional techniques such as neuraxial blocks, lumbar plexus block, femoral nerve block, fascia iliac block and intraarticular local anesthetic injection have been used for the treatment of acute postoperative pain.

Femoral nerve and fascia iliac blocks have shown good results for long-term post-surgery analgesia. However, the obturator nerve and accessory obturator nerve should be targeted to achieve more effective perioperative pain control. There are studies reporting that pericapsular nerve group block (PENG), which has been defined in recent years, provides effective perioperative analgesia in hip surgeries. In this study, we aim to compare the effectiveness of PENG block and intra-articular local anesthetic injection in hip arthroscopy.

Registry
clinicaltrials.gov
Start Date
January 20, 2021
End Date
April 2024
Last Updated
2 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Serdar Yeşiltaş

Assist Prof

Bezmialem Vakif University

Eligibility Criteria

Inclusion Criteria

  • American Association of Anesthesiologists (ASA) physical status I - III
  • BMI 20 to 35 kg / m2
  • Patients scheduled for elective hip arthroscopy
  • Able to provide informed consent.

Exclusion Criteria

  • Patients who refuse to participate in the study,
  • Coagulopathy,
  • Hepatic or renal insufficiency,
  • Pregnancy
  • Allergy to local anesthetic drugs,
  • Chronic pain condition requiring opioid intake at home,
  • BMI above
  • History of psychiatric diseases needing treatment.
  • Failure of nerve block
  • Substance abuse history

Outcomes

Primary Outcomes

Postoperative opioid consumption

Time Frame: up to the first 24 hours postoperatively

Total amount of morphine consumption during the first 24 hours after surgery. Patient controlled analgesia to be inserted.

Secondary Outcomes

  • Pain intensity score(0.5, 1, 3, 6, 12, 24 hours postoperatively.)
  • Postoperative nausea and vomiting(up to the first 24 hours postoperatively)
  • First rescue analgesic time(up to the first 24 hours postoperatively)
  • Patient satisfaction(at the end of 24 hours postoperatively)

Study Sites (1)

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