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Completed

NCT Number: NCT04681222

Comparison of the Efficacy of PENG Block in Combination With LFCN Block and Wound Infiltration

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.

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Key information

Conditions

Postoperative Pain Arthritis Joint Diseases Musculoskeletal Diseases Neurologic Manifestations Osteoarthritis Osteoarthritis, Hip Pain Pain, Postoperative Pathologic Processes Pathological Conditions, Signs and Symptoms Postoperative Complications Rheumatic Diseases Signs and Symptoms

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Derince Training and Research Hospital

Kocaeli, Derince, 41900, Turkey (Türkiye)

About this study

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.

Who can participate

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

LFCN

Procedure

LFCN block was performed in combination with PENG block

Wound Infiltration

Procedure

Wound infiltration was performed in combination with PENG block

Primary outcomes

  1. First analgesic demand

    Time frame: 24 hours

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

Secondary outcomes

  1. Opioid consumption

    Time frame: 24 hours

    Total opioid analgesic consumption

  2. Numeric Rating Scale

    Time frame: 24 hours

    The maximum score on a 10cm numeric rating scale: (0 to 10cm) (0 = no pain, 10 = worst imaginable pain)

  3. Nonsteroidal Anti-inflammatory Drugs (NSAID)

    Time frame: 24 hours

    Total NSAID consumption

Sponsors and collaborators

Lead sponsor

Derince Training and Research Hospital

Other

Collaborators

  • Bursa Yuksek Ihtisas Training and Research Hospital

Registry information

Official study title

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

Important dates

Study start
2019
Primary completion
2019
Study completion
2019
First posted
Dec 23, 2020
Registry last updated
Dec 24, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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