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Clinical Trials/NCT06457880
NCT06457880
Completed
Not Applicable

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

Campus Bio-Medico University1 site in 1 country40 target enrollmentJanuary 1, 2022

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Hip Fractures
Sponsor
Campus Bio-Medico University
Enrollment
40
Locations
1
Primary Endpoint
preoperative pain
Status
Completed
Last Updated
last year

Overview

Brief Summary

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.

Registry
clinicaltrials.gov
Start Date
January 1, 2022
End Date
June 1, 2024
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Campus Bio-Medico University
Responsible Party
Principal Investigator
Principal Investigator

Francesca Gargano

Medical director, Anesthesiologist

Campus Bio-Medico University

Eligibility Criteria

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

Outcomes

Primary Outcomes

preoperative pain

Time Frame: 30 minutes

Preoperative pain score expressed by numerical rating scale 0-10

Pain following regional anesthesia

Time Frame: 30 minutes

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

Postoperative pain

Time Frame: 24 hours

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

Secondary Outcomes

  • Morphine milligrams (mg) consumption(24 hours)

Study Sites (1)

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