Elevated Rate Pacing of Cardiac Amyloidosis
Recruiting now · Not applicable
Conditions studied: Cardiac Amyloidosis, Pacemaker
In brief
This study aims to better quantify the improvements in heart failure symptoms and exercise tolerance before and after the heart rate elevation in a cohort of 10 cardiac amyloidosis patients with preexisting pacemakers.
Key facts
- Study ID
- NCT07583823
- Run by
- University of Minnesota
- People needed
- 10
- Starts
- 2025-10-10
- Expected to finish
- 2026-10-10
- Last updated by the study team
- 2026-05-13
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Adults 18 and older
- Diagnosis of cardiac amyloidosis as indicated by the criteria set forth in guidelines such as in Kittleson et al: "2023 ACC Expert Consensus Decision Pathway on Comprehensive Multidisciplinary Care for the Patient With Cardiac Amyloidosis: A Report of the American College of Cardiology Solution Set Oversight Committee
- Implanted Cardiac Pacemaker (+/- Defibrillator)
- Pacemaker mode of AAI or DDD if in sinus rhythm, VVI acceptable if permanent atrial fibrillation
- Non-dilated left ventricle by echocardiography
- Ability to provide written consent
- English Speaking
You may not qualify if…
- Paced QRS duration of >150 ms (indicator for pacing mediated dyssynchrony)
- Dilated left ventricle
Where it is running
- University of Minnesota — Minneapolis, Minnesota, United States (enrolling)
Full record on ClinicalTrials.gov
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