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Clinical Trials/NCT04996290
NCT04996290
Completed
Not Applicable

Combined Pericapsular Nerve Group (PENG) and Lateral Femoral Cutaneous Nerve (LFCN) Block for Total Hip Arthroplasty: A Randomized Controlled Trial

University Hospital, Antwerp1 site in 1 country40 target enrollmentJune 1, 2020

Overview

Phase
Not Applicable
Intervention
PENG + LFCN block
Conditions
Anesthesia, Conduction
Sponsor
University Hospital, Antwerp
Enrollment
40
Locations
1
Primary Endpoint
Initial pain score
Status
Completed
Last Updated
4 years ago

Overview

Brief Summary

A clinical trial investigating the effect of a combined locoregional anesthesia technique on the postoperative analgesia outcomes after a total hip arthroplasty. A PENG block will be used in combination with a LFCN block. The results will be compared to a control group that is solely treated with intravenous analgesia. This technique aims to provide improved pain scores after surgery without interference of revalidation.

Registry
clinicaltrials.gov
Start Date
June 1, 2020
End Date
October 1, 2020
Last Updated
4 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Lennert De Schrijver

Principal Investigator

University Hospital, Antwerp

Eligibility Criteria

Inclusion Criteria

  • adult patients who underwent a primary total hip replacement under general anesthesia

Exclusion Criteria

  • insulin dependent diabetes mellitus
  • chronic pain
  • severe dementia or mental retardation
  • allergy to local anesthetics

Arms & Interventions

PENG + LFCN block

The participants in this group received a combined regional technique just before surgery: * Pericapsular nerve group (PENG) block * Lateral femoral cutaneus nerve (LFCN) block

Intervention: PENG + LFCN block

PENG + LFCN block

The participants in this group received a combined regional technique just before surgery: * Pericapsular nerve group (PENG) block * Lateral femoral cutaneus nerve (LFCN) block

Intervention: Ropivacaine injection

Outcomes

Primary Outcomes

Initial pain score

Time Frame: 0 hours postoperative

numeric rating score (NRS) of 0 to 10

Pain score after 2h

Time Frame: 2 hours postoperative

numeric rating score (NRS) of 0 to 10

Pain score after 24h

Time Frame: 24 hours postoperative

numeric rating score (NRS) of 0 to 10

Secondary Outcomes

  • Initial motor function(0 hours postoperative)
  • Motor function after 2h(2 hours postoperative)
  • Postoperative opioids(24 hours postoperative)
  • Intraoperative opioids(intraoperative)
  • Motor function after 24h(24 hours postoperative)

Study Sites (1)

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