RECRUITING

Aveir VR Coverage With Evidence Development Post-Approval Study

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 purpose of this coverage with evidence development (CED) study is to evaluate complications and long-term health outcomes of the single-chamber Aveir Single-Chamber Leadless Pacemaker device (Aveir VR LP).

Official Title

Aveir Single-Chamber Leadless Pacemaker Coverage With Evidence Development (ACED) Post-Approval Study

Quick Facts

Study Start:2022-06-21
Study Completion:2028-01-01
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT05336877

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:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. Age 18 years or older
  2. Willing and able to provide informed consent
  3. Able to understand and follow study procedures
  4. Stable medical condition
  1. Pregnancy or breastfeeding
  2. Severe psychiatric disorders
  3. Active substance abuse
  4. Unstable medical conditions
  5. Inability to comply with study requirements

Contacts and Locations

Study Contact

Grant Kim
CONTACT
818-493-3147
Grant.kim1@abbott.com
Binh Ngo
CONTACT
8184932060
binh.ngo1@abbott.com

Principal Investigator

Grant Kim
STUDY_DIRECTOR
Abbott

Study Locations (Sites)

Abbott
Sylmar, California, 91342
United States

Collaborators and Investigators

Sponsor: Abbott Medical Devices

  • Grant Kim, STUDY_DIRECTOR, Abbott

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 Date2022-06-21
Study Completion Date2028-01-01

Study Record Updates

Study Start Date2022-06-21
Study Completion Date2028-01-01

Terms related to this study

Additional Relevant MeSH Terms

  • Cardiac Pacemaker
  • Arrythmia
  • Bradycardia