RECRUITING

Cryoablation Effects on Acute and Chronic Pain After Thoracotomy and Thoracoscopy

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

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.

Official Title

Cryoablation Effects on Acute and Chronic Pain After Thoracotomy and Thoracoscopy

Quick Facts

Study Start:2024-06-03
Study Completion:2028-04
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06384664

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Patients who could receive cryoablation in an elective open thoracic (posterolateral thoracotomy) or minimally invasive (thoracoscopy, including robotic) procedures at Michigan Medicine
  2. * Patient is opioid naïve
  1. * Patients who are pregnant
  2. * Patients with cognitive impairment
  3. * Patients with psychological disorders
  4. * Patients with prior thoracic surgery
  5. * Patients with fibromyalgia
  6. * Patients with redo ipsilateral thoracic surgery
  7. * Patients undergoing bilateral thoracotomy

Contacts and Locations

Study Contact

Shari L Barnett
CONTACT
734-936-4561
shbailey@umich.edu

Principal Investigator

Rishindra Reddy, MD, MBA
PRINCIPAL_INVESTIGATOR
University of Michigan

Study Locations (Sites)

University of Michigan
Ann Arbor, Michigan, 48109
United States

Collaborators and Investigators

Sponsor: University of Michigan

  • Rishindra Reddy, MD, MBA, PRINCIPAL_INVESTIGATOR, University of Michigan

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2024-06-03
Study Completion Date2028-04

Study Record Updates

Study Start Date2024-06-03
Study Completion Date2028-04

Terms related to this study

Additional Relevant MeSH Terms

  • Pain, Postoperative
  • Intrathoracic Procedure