Cryoablation Effects on Acute and Chronic Pain After Thoracotomy and Thoracoscopy
University of Michigan · with AtriCure, Inc. · NCT06384664
Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.
Key facts
- Compensation
- Not posted. Ask the study team before screening.
- Who can join
- Ages 18+ · All sexes
- Healthy volunteers
- Accepted
- Study type
- Interventional · Not applicable
- Target enrollment
- 80
- US sites recruiting
- 1
- Study start
- June 3, 2024
- Record last updated
- August 28, 2025
Status re-checked against ClinicalTrials.gov within the last 12 hours.
What the study is about
The researchers will compare the common methods of post-surgical pain control, such as epidural or intercostal nerve block with a newer method called cryoablation. The research team is conducting this study to determine if cryoablation provides more effective pain control when compared to an epidural or intercostal nerve block.
Being studied: Atricure's crysoSPHERE probe; Standard of Care
Conditions: Pain, Postoperative; Intrathoracic Procedure
Eligibility criteria
Copied from the official record. The study team makes the final decision at screening.
Show full criteria
Inclusion Criteria
- Patients who could receive cryoablation in an elective open thoracic (posterolateral thoracotomy) or minimally invasive (thoracoscopy, including robotic) procedures at Michigan Medicine
- Patient is opioid naïve
Exclusion Criteria
- Patients who are pregnant
- Patients with cognitive impairment
- Patients with psychological disorders
- Patients with prior thoracic surgery
- Patients with fibromyalgia
- Patients with redo ipsilateral thoracic surgery
- Patients undergoing bilateral thoracotomy
Recruiting US locations
University of Michigan
Ann Arbor, MI 48109
Site contact: Shari L Barnett · 734-936-4561 · shbailey@umich.edu
Study contacts (from the official record)
- Shari L Barnett · 734-936-4561 · shbailey@umich.edu
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