Randomized Control Trial, Cryoablation as an Adjunct to Surgical Stabilization of Rib Fractures (NCT05415384)
Single Center, Randomized Control Trial of Cryoablation During Surgical Stabilization of Rib Fractures
🩺 Plain-English Summary (8th-Grade Level)
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
Who can join: Review the eligibility criteria below.
Location: Wake Forest University Health Sciences — Winston-Salem, North Carolina
Age range: 18 Years to 80 Years
🧪 Interventions in This Study
📋 "Do I Qualify?" — 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria ↗
📍 All Participating Trial Locations (1 Sites)
- Wake Forest University Health Sciences — Winston-Salem, North Carolina
📞 Contact the Study Coordinator
Phone: (704) 355-3176
Email: Bradley.Thomas@wfusm.edu
Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.
💰 Cost, Insurance & Patient Rights
- 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
- Routine Patient Care: Under federal law (ACA § 2709) and many state statutes, routine care costs are covered during participation.
- Voluntary Participation: You may withdraw at any time without affecting your standard medical care.
More studies in Pain, Postoperative
- Comprehensive Study of Post-surgical Pain After Pectus or Spine Surgery — Cincinnati, Ohio
- A Prospective Randomized Double Blind Trial to Assess the Effect of a Single Preoperative Dose of Gabapentin on Postoperative Opioid Consumption in Patients Undergoing Rhinoplasty — Columbus, Ohio
- Stopping Opioid Overuse in Obstetrics to Halt Exposure Trial — Kansas City, Missouri
- Reduced Opioid Prescription After Laparoscopic Hysterectomy — Baltimore, Maryland
- Magnesium as an Adjuvant Agent for Postoperative Pain — Cleveland, Ohio
- Personalization of Opioid Prescription Following Orthognathic Surgery — Halifax, Nova Scotia
Explore by condition: All Pain, Postoperative clinical trials
💡 How to Participate
- Check the checklist above to see if you may qualify.
- Contact the study coordinator using the phone/email above.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.