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Clinical Trials/NCT04681222
NCT04681222
Completed
Not Applicable

Postoperative Pain Management in Patients Undergoing Total Hip Arthroplasty: PENG Block in Combination With LFCN Block or Wound Infiltration?

Derince Training and Research Hospital1 site in 1 country22 target enrollmentJanuary 1, 2019

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Postoperative Pain
Sponsor
Derince Training and Research Hospital
Enrollment
22
Locations
1
Primary Endpoint
First analgesic demand
Status
Completed
Last Updated
5 years ago

Overview

Brief Summary

The ultrasound-guided approach for the blockade of articular branches of femoral and obturator nerves, pericapsular nerve group (PENG) block, is an effective method for postoperative analgesia in hip surgeries.

Detailed Description

The ultrasound-guided approach for the blockade of articular branches of femoral and obturator nerves, pericapsular nerve group (PENG) block, is an effective method for postoperative analgesia in hip surgeries. However, it fails to provide cutaneous analgesia on the anterolateral surgical incisional site. This study compares the effects of wound infiltration and lateral femoral nerve blocks in combination with PENG blocks for postoperative pain in patients undergoing total hip arthroplasty for coxarthrosis.

Registry
clinicaltrials.gov
Start Date
January 1, 2019
End Date
December 31, 2019
Last Updated
5 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
Derince Training and Research Hospital
Responsible Party
Principal Investigator
Principal Investigator

Hande Gurbuz

Medical Doctor, Associate Professor, Principal Investigator

Derince Training and Research Hospital

Eligibility Criteria

Inclusion Criteria

  • Coxarthrosis
  • Total hip replacement
  • Patients agreed to receive PENG block
  • LFCN or wound infiltration performed combined with PENG blocks

Exclusion Criteria

  • Other kinds of hip surgeries
  • Total hip replacement performed for other indications
  • Patients refused to receive PENG block

Outcomes

Primary Outcomes

First analgesic demand

Time Frame: 24 hours

The time interval from PENG blocks to the first analgesic demand.

Secondary Outcomes

  • Numeric Rating Scale(24 hours)
  • Nonsteroidal Anti-inflammatory Drugs (NSAID)(24 hours)
  • Opioid consumption(24 hours)

Study Sites (1)

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