Clinical Trials Directory

Trials / Recruiting

RecruitingNCT06347874

Cryo Rib Fracture Study

Comparison of Cryoablation of Intercostal Nerves to Erector Spinae Plane Catheters in Patients With Rib Fractures

Status
Recruiting
Phase
Phase 4
Study type
Interventional
Enrollment
48 (estimated)
Sponsor
University of Minnesota · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to determine if patients with rib fractures who undergo cryoablation of the intercostal nerves have improved pain control 7 days from procedure when compared to those who have a ESP catheter.

Conditions

Interventions

TypeNameDescription
DRUGCryoablationan injection of 1ml of 1% lidocaine per rib and ultrasound guided cryoablation of the intercostal nerves
DRUGESP Catheteran ultrasound guided erector spinae plane catheter with initial bolus of 30 mL of 0.25% bupivacaine followed by infusion of 0.2% ropivacaine at 10 mL per hour via programmed intermittent bolus.

Timeline

Start date
2025-01-10
Primary completion
2027-02-13
Completion
2027-03-13
First posted
2024-04-04
Last updated
2026-02-17

Locations

1 site across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT06347874. Inclusion in this directory is not an endorsement.

Cryo Rib Fracture Study (NCT06347874) · Clinical Trials Directory