RECRUITING

Impella RP Flex with Smart Assist

Talk to us

Conditions

Right Ventricular (RV) Dysfunction

Quick Navigation

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

To capture observational data of the Abiomed Impella RP Flex in a real-world setting.

Official Title

Impella RP Flex Registry

Quick Facts

Study Start:2024-05-29
Study Completion:2026-06-01
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06637644

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:Not specified
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:CHILD, ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Subjects who received mechanical circulatory support (MCS) with an Impella RP Flex will be considered eligible for the registry.
  1. * None

Contacts and Locations

Study Contact

Stacie Hallaway, Sr. Clinical Project Manager
CONTACT
839-216-3087
shallawa@its.jnj.com

Study Locations (Sites)

University of Alabama at Birmingham
Birmingham, Alabama, 35294
United States
Pima Heart and Vascular
Tucson, Arizona, 85718
United States
Baptist Health Heart Failure and Transplant Institute
Little Rock, Arkansas, 72205
United States
Arkansas Heart Hospital
Little Rock, Arkansas, 72211
United States
University of Southern California (Keck USC)
Los Angeles, California, 90033
United States
Advent Health Orlando
Orlando, Florida, 32803
United States
Tampa General
Tampa, Florida, 33606
United States
Ochsner Clinic Foundation
New Orleans, Louisiana, 70121
United States
Beth Israel Deaconess Medical Center
Boston, Massachusetts, 02215
United States
Henry Ford Hospital
Detroit, Michigan, 48202
United States
Ascension St. John Hospital
Detroit, Michigan, 48236
United States
Metropolitan Heart and Vascular Institute
Coon Rapids, Minnesota, 55433
United States
Providence St. Patrick Hospital
Missoula, Montana, 59802
United States
University of Nebraska Medical Center
Omaha, Nebraska, 68198
United States
Rutgers Robert Wood Johnson Medical School
New Brunswick, New Jersey, 08901
United States
Montefiore Medical Center - Moses
Bronx, New York, 10467
United States
Northwell Health/Lenox Hill Hospital
New York, New York, 10075
United States
Novant Health New Hanover Regional Medical Center
Wilmington, North Carolina, 28401
United States
Wake Forest University School of Medicine
Winston-Salem, North Carolina, 27101
United States
The Lindner Research Center at the Christ Hospital
Cincinnati, Ohio, 45219
United States
Providence St. Vincent Medical Center
Portland, Oregon, 97225
United States
Legacy Research Institute (Legacy Emanuel Medical Center)
Portland, Oregon, 97232
United States
Oregon Health and Science System
Portland, Oregon, 97239
United States
UPMC Presbyterian
Pittsburgh, Pennsylvania, 15213
United States
Medical City Heart Hospital Dallas
Dallas, Texas, 75243
United States
Baylor University Medical Center
Dallas, Texas, 75246
United States
Memorial Herman Texas Medical Center
Houston, Texas, 77030
United States
The Heart Hospital Baylor Plano
Plano, Texas, 75093
United States
MultiCare Institute for Research Innovation
Puyallup, Washington, 98372
United States
Providence Sacred Heart Medical Center
Spokane, Washington, 99204
United States
Froedtert Hospital (Medical College of Wisconsin)
Milwaukee, Wisconsin, 53226
United States

Collaborators and Investigators

Sponsor: Abiomed Inc.

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 Date2024-05-29
Study Completion Date2026-06-01

Study Record Updates

Study Start Date2024-05-29
Study Completion Date2026-06-01

Terms related to this study

Additional Relevant MeSH Terms

  • Right Ventricular (RV) Dysfunction