RECRUITING

A Multicenter Patient Registry on Outcomes From Cryoanalgesia of the Intercostal Nerves

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

This is a retrospective and prospective, multicenter, observational patient registry to record outcomes from patients undergoing cryoablation of the intercostal nerves (cryoanalgesia) for post-operative pain management.

Official Title

The CryoICE™ Cryoanalgesia Registry for Pain Management in Post-cardiothoracic Surgery Via Cryoablation of the Intercostal Nerves

Quick Facts

Study Start:2018-06-29
Study Completion:2040-01
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT05110989

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:12 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:CHILD, ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. 1. Patients whose age is 12 years or above, and are able to give informed consent/assent specific to state and national law.
  2. 2. Patients have been scheduled by physician(s) to undergo or have undergone cryoablation of the intercostal nerves utilizing at least one AtriCure device or are similar patients treated without the use of cryoablation
  1. 1. Patient is enrolled in a concurrent trial that may impact the treatment offered by the registry devices.
  2. 2. Patient with exclusion criteria required by local governance.
  3. 3. Women of childbearing potential who are, or plan to become, pregnant during the time of the study

Contacts and Locations

Study Contact

Elizabeth Menard
CONTACT
8327120715
REDUCE-REGISTRY@atricure.com
Laura O'Brien, PhD
CONTACT
763-310-6151
lobrien@atricure.com

Principal Investigator

Curits Quinn, MD
PRINCIPAL_INVESTIGATOR
Elliot Hospital

Study Locations (Sites)

AdventHealth
Orlando, Florida, 32803
United States
Henry Ford Health Rochester Hospital
Rochester, Michigan, 48307
United States
St. Luke's Hospital of Kansas City
Kansas City, Missouri, 64111
United States
Elliot Hospital
Manchester, New Hampshire, 03101
United States
The Christ Hospital
Cincinnati, Ohio, 45219
United States
Baylor College of Medicine
Houston, Texas, 77030
United States

Collaborators and Investigators

Sponsor: AtriCure, Inc.

  • Curits Quinn, MD, PRINCIPAL_INVESTIGATOR, Elliot Hospital

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 Date2018-06-29
Study Completion Date2040-01

Study Record Updates

Study Start Date2018-06-29
Study Completion Date2040-01

Terms related to this study

Additional Relevant MeSH Terms

  • Post Operative Pain