Condition: Aortic Stenosis · Hypo-attenuated Leaflet Thickening · Bioprosthetic Valve Degeneration · Sponsor: Massachusetts General Hospital
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…
This description comes directly from the study's public registry record.
Roukoz Abou Karam · raboukaram@mgh.harvard.edu
Paris J Jamiel, BS · (617) 726-0996 · pjamiel@mgh.harvard.edu
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| Massachusetts General Hospital | Boston, Massachusetts, United States | Recruiting |
| Minneapolis Heart Institute | Minneapolis, Minnesota, United States | Not Yet Recruiting |
| Catholic Medical Center | Manchester, New Hampshire, United States | Recruiting |
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Source record: clinicaltrials.gov/study/NCT04552275