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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03232736
Other study ID # 17-1042
Secondary ID
Status Completed
Phase
First received
Last updated
Start date October 1, 2017
Est. completion date January 30, 2020

Study information

Verified date November 2023
Source University of Colorado, Denver
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The primary reason the investigators are doing this study are to understand how the right side of the heart functions in heart failure patients with left ventricular assist devices (LVADs, or "mechanical hearts"). Second, the investigators are interested in understanding how different pacemaker settings influence function of the heart at rest and activity.


Description:

Healthy individuals, as well as patients with advanced heart failure supported by LVADs, completed invasive hemodynamic analysis at rest and with exercise to characterize right-sided heart function at rest and with exercise during invasive cardiopulmonary exercise testing on upright cycle ergometry.


Recruitment information / eligibility

Status Completed
Enrollment 22
Est. completion date January 30, 2020
Est. primary completion date January 30, 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 80 Years
Eligibility 15 patients with advanced heart failure (HF) who have already undergone implantation of a continuous-flow left ventricular assist device (CF-LVAD) implantation. Inclusion criteria: 1. Have already received CF-LVADs and are clinically stable, 2. Ambulatory outpatients and are fully recovered (at least 3 months) from LVAD implantation; Exclusion criteria: 1. Individuals with clinical right ventricular (RV) failure under resting conditions, defined as moderate-severely reduced RV systolic function on echocardiography, or 2. Clinical evidence of RV failure (elevated jugular venous pressures, 3 or 4+ [significant] peripheral edema); 3. Disorders that adversely influence exercise ability (e.g. arthritis, peripheral vascular disease, pulmonary disease); and 10 healthy individuals will serve as a control group to define normal RV function during exercise. Inclusion criteria: 1) Persons without a past medical history of cardiovascular disease or related disease such as: 1. hypertension, 2. diabetes, 3. peripheral vascular disease, 4. arrhythmias, f. are not taking any cardiac-related medications (e.g. antihypertensive medications). Exclusion criteria: 1. Individuals requiring systemic anticoagulation with vitamin-K antagonists or new/direct oral anticoagulants ("NOAC"/"DOAC"); 2. Disorders that adversely influence exercise ability (e.g. arthritis, peripheral vascular disease).

Study Design


Locations

Country Name City State
United States University of Colorado Hospital Aurora Colorado

Sponsors (1)

Lead Sponsor Collaborator
University of Colorado, Denver

Country where clinical trial is conducted

United States, 

References & Publications (2)

Cornwell WK, Tran T, Cerbin L, Coe G, Muralidhar A, Hunter K, Altman N, Ambardekar AV, Tompkins C, Zipse M, Schulte M, O'Gean K, Ostertag M, Hoffman J, Pal JD, Lawley JS, Levine BD, Wolfel E, Kohrt WM, Buttrick P. New insights into resting and exertional right ventricular performance in the healthy heart through real-time pressure-volume analysis. J Physiol. 2020 Jul;598(13):2575-2587. doi: 10.1113/JP279759. Epub 2020 May 18. — View Citation

Tran T, Muralidhar A, Hunter K, Buchanan C, Coe G, Hieda M, Tompkins C, Zipse M, Spotts MJ, Laing SG, Fosmark K, Hoffman J, Ambardekar AV, Wolfel EE, Lawley J, Levine B, Kohrt WM, Pal J, Cornwell WK 3rd. Right ventricular function and cardiopulmonary performance among patients with heart failure supported by durable mechanical circulatory support devices. J Heart Lung Transplant. 2021 Feb;40(2):128-137. doi: 10.1016/j.healun.2020.11.009. Epub 2020 Nov 22. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Peak Vo2 peak Vo2 measured by indirect calorimetry during cardiopulmonary exercise testing 20 minutes
Primary Cardiac Output cardiac output measured during invasive cardiopulmonary exercise testing. 20 minutes
Secondary Blood Pressure mean arterial pressure during exercise 20 minutes
Secondary Respiratory Exchange Ratio Respiratory exchange ratio derived from indirect calorimetry 20 minutes
Secondary Minute Ventilation Minute ventilation during cardiopulmonary exercise testing 20 minutes
Secondary Tau unit of measure of diastolic function during exercise 20 minutes
Secondary Stroke Work stroke work during exercise 20 minutes
Secondary EES/EA ventricular arterial coupling during exercise 20 minutes
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