RECRUITING

The HALT Biomarker 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 the HALT Biomarkers study are to identify a panel of circulating proteins that discriminates between patients with and without Hypo-Attenuated Leaflet Thickening (HALT) and can be used to supplement the diagnosis of HALT; to characterize changes in circulating proteins after treatment of HALT with systemic anticoagulation; and to identify circulating proteins that predict the occurrence of HALT. The study population will be adult patients undergoing transfemoral transcatheter aortic valve replacement (TAVR) for severe aortic stenosis (AS) or bioprosthetic valve degeneration. Enrollment will continue until 30 patients with HALT are identified for completion of phase 1. Based on a HALT incidence rate of 10%, we anticipate enrolling 300 patients. Patients are enrolled prior to undergoing transfemoral TAVR. Blood samples, clinical data and echocardiograms will be collected at the following timepoints: baseline (pre-TAVR, T0), post-TAVR (pre-discharge, T1), 30-day follow-up (window 3-9 weeks, T2), and 6-month follow-up (T3). Cardiac 4D CT will be performed at the 30-day follow-up visit to screen for the occurrence of HALT. Patients with HALT will be treated with systemic anticoagulation for 5-6 months, at which point a follow-up CT scan and blood sample will be obtained. Control subjects will also undergo a 6-month study visit with blood sample collection. The study will be conducted within two phases. Phase 1 will serve as a derivation / discovery study in which candidate protein biomarkers of HALT will be identified. Once this is successfully completed, a second cohort will be enrolled within phase 2. Phase 2 will be performed under the auspices a future contract or amendment and will seek to cross-validate the initial study findings.

Official Title

Circulating Biomarkers of Hypo-Attenuated Leaflet Thickening After Transcatheter Aortic Valve Replacement

Quick Facts

Study Start:2020-06-22
Study Completion:2035-06-22
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT04552275

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:65 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. 1. Age \> 65 years
  2. 2. Subject with severe native AS or severe bioprosthetic valve degeneration
  3. 3. Subject undergoing transfemoral TAVR using a Medtronic Evolut R, Evolut Pro or Evolut Pro+ transcatheter heart valve
  1. 1. Chronic anticoagulation therapy
  2. 2. Contraindication to systemic oral anticoagulation therapy
  3. 3. Chronic kidney disease with EGFR\<30 ml/min
  4. 4. Bleeding diathesis or known coagulopathy
  5. 5. Hypercoagulable state
  6. 6. Life-expectancy \<12 months due to other medical conditions (e.g., malignancy, severe Alzheimer's disease, etc.)
  7. 7. The patient is currently participating in another investigational device or drug study that has not reached its primary objective/endpoint
  8. 8. Pregnant, lactating, or planning pregnancy within next 12 months

Contacts and Locations

Study Contact

Roukoz Abou Karam
CONTACT
raboukaram@mgh.harvard.edu
Paris J Jamiel, BS
CONTACT
(617) 726-0996
pjamiel@mgh.harvard.edu

Study Locations (Sites)

Massachusetts General Hospital
Boston, Massachusetts, 02114
United States
Minneapolis Heart Institute
Minneapolis, Minnesota, 55407
United States
Catholic Medical Center
Manchester, New Hampshire, 03103
United States

Collaborators and Investigators

Sponsor: Massachusetts General 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 Date2020-06-22
Study Completion Date2035-06-22

Study Record Updates

Study Start Date2020-06-22
Study Completion Date2035-06-22

Terms related to this study

Additional Relevant MeSH Terms

  • Aortic Stenosis
  • Hypo-attenuated Leaflet Thickening
  • Bioprosthetic Valve Degeneration