Actively Recruiting

Phase Not Applicable
Age: 18Years - 80Years
All Genders
NCT05415384

Randomized Control Trial, Cryoablation as an Adjunct to Surgical Stabilization of Rib Fractures

Led by Wake Forest University Health Sciences · Updated on 2026-03-16

80

Participants Needed

1

Research Sites

213 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

To determine if patients with intraoperative cryoablation have better analgesia results compared to the control group of Surgical Stabilization of Rib Fractures (SSRF) without cryoablation

CONDITIONS

Official Title

Randomized Control Trial, Cryoablation as an Adjunct to Surgical Stabilization of Rib Fractures

Who Can Participate

Age: 18Years - 80Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patient admitted to trauma service
  • Multiple displaced rib fractures (2 or more ribs) and consents to surgical stabilization of rib fractures (SSRF)
  • Not currently treated for chronic pain
  • Age above 18 years and below 80 years
  • Surgery planned within 120 hours from injury
Not Eligible

You will not qualify if you...

  • Age below 18 years or 80 years and above
  • Flail chest defined by CT or clinical exam
  • Moderate or severe traumatic brain injury with Glasgow Coma Scale below 12
  • Prior or expected emergency exploratory laparotomy, thoracotomy, or craniotomy during admission
  • Spinal cord injury
  • Pelvic fracture requiring or expected to require surgery during admission
  • Unable to perform daily living activities independently before injury
  • Incarceration
  • Known pregnancy
  • Unable to perform Video Assisted Thoracoscopy (VATS) at time of surgery due to lung issues or previous pathology

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Wake Forest University Health Sciences

Winston-Salem, North Carolina, United States, 27157

Actively Recruiting

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Research Team

B

Bradely W Thomas, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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