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Cryoablation Effects on Acute and Chronic Pain After Thoracotomy and Thoracoscopy

RecruitingNot applicableNCT06384664
View the official record on ClinicalTrials.gov

Recruiting status changes often. Contact the study team listed on ClinicalTrials.gov, and talk to your doctor before joining a study.

This study has no listed site in Canada in this snapshot. It is included as part of the worldwide chronic pain corpus.

Brief summary (from the registry)

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.

Study details

Official title
Cryoablation Effects on Acute and Chronic Pain After Thoracotomy and Thoracoscopy
Conditions
Interventions
  • Device: Atricure's crysoSPHERE probe
  • Procedure: Standard of Care
Sponsor
University of Michigan
Collaborators
AtriCure, Inc.
Start date
2024-06-03
Primary completion
2027-04
Sex
All
Age range
from 18 Years
Healthy volunteers
true
Results posted
No results posted in this snapshot
Countries
United States
Total sites listed
1

Eligibility criteria

Show eligibility criteria (verbatim from the registry)
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

Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT06384664