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

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.

Conditions

Post Operative Pain

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Study Overview

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Study Details

Study overview

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.

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

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

Condition
Post Operative Pain
Intervention / Treatment

-

Contacts and Locations

Orlando

AdventHealth, Orlando, Florida, United States, 32803

Rochester

Henry Ford Health Rochester Hospital, Rochester, Michigan, United States, 48307

Kansas City

St. Luke's Hospital of Kansas City, Kansas City, Missouri, United States, 64111

Manchester

Elliot Hospital, Manchester, New Hampshire, United States, 03101

Cincinnati

The Christ Hospital, Cincinnati, Ohio, United States, 45219

Houston

Baylor College of Medicine, Houston, Texas, United States, 77030

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.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • 1. Patients whose age is 12 years or above, and are able to give informed consent/assent specific to state and national law.
  • 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. Patient is enrolled in a concurrent trial that may impact the treatment offered by the registry devices.
  • 2. Patient with exclusion criteria required by local governance.
  • 3. Women of childbearing potential who are, or plan to become, pregnant during the time of the study

Ages Eligible for Study

12 Years to

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

AtriCure, Inc.,

Curits Quinn, MD, PRINCIPAL_INVESTIGATOR, Elliot Hospital

Study Record Dates

2040-01