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OpenTrials
Completed

NCT Number: NCT06457880

PENG Block vs FNB + ONB in Patients Undergoing Hip Fracture Surgery With Contraindications to Neuraxial Anesthesia

The aim of the study is to demonstrate the efficacy of PENG block as the main anesthetic technique to manage perioperative analgesia for hip fracture surgery compared to femoral and obturator nerve block in patients with contraindications to spinal anesthesia.

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Key information

Conditions

Hip Fractures Cardiovascular Diseases Coagulopathy Comorbidities and Coexisting Conditions Femoral Fractures Fractures, Bone Hematologic Diseases Hemic and Lymphatic Diseases Hemorrhagic Disorders Hemostatic Disorders Hip Injuries Leg Injuries Neurologic Manifestations Pain Pain, Postoperative Pathologic Processes Pathological Conditions, Signs and Symptoms Postoperative Complications Signs and Symptoms Vascular Diseases Wounds and Injuries

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Campus Bio Medico

Roma, 00128, Italy

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • patients undergo hip surgery
  • patients with contraindications at spinal anesthesia

Exclusion criteria

  • allergy at local anesthetic
  • age under 18 or weight under 30

Treatment and study plan

PENG block

Procedure

Preoperative ultrasound guided PENG block (ropivacaine 0.5 % 20 mL)

Femoral Nerve Block

Procedure

Preoperative ultrasound guided femoral nerve block (ropivacaine 0.5 % 15 mL)

Obturator nerve block

Procedure

Preoperative ultrasound guided obturator nerve block (ropivacaine 0.5 % 5 mL)

Primary outcomes

  1. preoperative pain

    Time frame: 30 minutes

    Preoperative pain score expressed by numerical rating scale 0-10

  2. Pain following regional anesthesia

    Time frame: 30 minutes

    Preoperative pain score following regional anesthesia execution expressed by numerical rating scale 0-10

  3. Postoperative pain

    Time frame: 24 hours

    Postoperative pain score expressed by a numerical rating scale 0-10

Secondary outcomes

  1. Morphine milligrams (mg) consumption

    Time frame: 24 hours

    needed opioid rescue therapy

Sponsors and collaborators

Lead sponsor

Campus Bio-Medico University

Other

Registry information

Official study title

Pericapsular Nerve Group (PENG) Block vs Femoral Nerve Block (FNB) + Obturator Nerve Block (ONB) in Patients Undergoing Hip Fracture Surgery With Contraindications to Neuraxial Anesthesia

Acronym: PENG/FNB+ONB

Important dates

Study start
2022
Primary completion
2023
Study completion
2024
First posted
Jun 13, 2024
Registry last updated
Jun 14, 2024

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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