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Comparison of Cryoablation of Pericapsular Nerve Group (PENG) to Fascia Iliaca Catheter in Patients With a Hip Fracture

University of Minnesota (UMN) logo

University of Minnesota (UMN)

Status and phase

Enrolling
Phase 4

Conditions

Hip Fractures

Treatments

Drug: fascia iliaca compartment block
Drug: PENG block and cryoablation

Study type

Interventional

Funder types

Other

Identifiers

NCT06278987
ANES-2024-32661

Details and patient eligibility

About

The purpose of this study is to determine if patients with hip fractures who undergo cryoablation of the PENG have improved pain control 30 days from surgery when compared to those who have a fascia iliaca catheter.

Enrollment

150 estimated patients

Sex

All

Ages

18 to 85 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients undergoing hip fracture repair aged 18-85.

Exclusion criteria

  • Patients who have an exclusion to regional anesthesia.
  • Patients who are pregnant assessed via self-report or pregnancy test if they have taken one.
  • Non-English speakers
  • Patients who already had their fracture repaired"

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

150 participants in 2 patient groups

PENG block and cryoablation
Experimental group
Description:
Patients undergoing hip fracture repair aged 18-85
Treatment:
Drug: PENG block and cryoablation
fascia iliaca compartment block
Experimental group
Description:
Patients undergoing hip fracture repair aged 18-85
Treatment:
Drug: fascia iliaca compartment block

Trial contacts and locations

1

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Central trial contact

Candace Nelson

Data sourced from clinicaltrials.gov

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