Randomized Control Trial, Cryoablation as an Adjunct to Surgical Stabilization of Rib Fractures
Recruiting
N/A
Interventional Study
Pain, Postoperative
Rib Fracture Multiple
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 – 80
- Sex
- Any
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 80 (estimated)
- Sponsor
- Wake Forest University Health Sciences · Other
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About This Trial
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
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* The patient is admitted to the trauma service.
* The patient has multiple displaced rib fractures (≥2 ribs), offered fixation, and consents to SSRF
* The patient is not being treated for chronic pain
* The patient is \>18 years of age.
* Surgery anticipated \<120 hours from in…
Contacts