RECRUITING

Baroreflex Activation Therapy in Left Ventricular Assist Device Patients Study

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Conditions

Congestive Heart FailureVentricular Assist DeviceBaroreflex activation therapy

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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 study will involve LVAD patients who have already received a clinically-indicated BAT (BAROSTIM) device. After recovery from LVAD implant, we will investigate the effects of BAT in a double-blind cross-over study design.

Official Title

Baroreflex Activation Therapy in Left Ventricular Assist Device Patients Study (BAT-VAD Study)

Quick Facts

Study Start:2024-02-01
Study Completion:2027-04-25
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06195046

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
  2. * LVAD patient \> 3 months post implant
  3. * Existing BAT device
  1. * Presence of cardiogenic shock, respiratory failure, hypotension or unstable heart failure
  2. * Bradycardia (resting HR \<60 beats/minute)
  3. * Presence of suspected pump thrombosis at the time of enrollment
  4. * Presence of any significant ventricular arrhythmias at the time of enrollment

Contacts and Locations

Study Locations (Sites)

Medical University of South Carolina
Charleston, South Carolina, 29425
United States

Collaborators and Investigators

Sponsor: Brian Houston

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 Date2024-02-01
Study Completion Date2027-04-25

Study Record Updates

Study Start Date2024-02-01
Study Completion Date2027-04-25

Terms related to this study

Keywords Provided by Researchers

  • Ventricular Assist Device
  • Baroreflex activation therapy

Additional Relevant MeSH Terms

  • Congestive Heart Failure