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Recruiting NCT06384664

NCT06384664 Cryoablation Effects on Acute and Chronic Pain After Thoracotomy and Thoracoscopy

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Clinical Trial Summary
NCT ID NCT06384664
Status Recruiting
Phase
Sponsor University of Michigan
Condition Pain, Postoperative
Study Type INTERVENTIONAL
Enrollment 80 participants
Start Date 2024-06-03
Primary Completion 2027-04

Trial Parameters

Condition Pain, Postoperative
Sponsor University of Michigan
Study Type INTERVENTIONAL
Phase N/A
Enrollment 80
Sex ALL
Min Age 18 Years
Max Age N/A
Start Date 2024-06-03
Completion 2027-04
Interventions
Atricure's crysoSPHERE probeStandard of Care

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Brief Summary

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.

Eligibility 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

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