A SkeleTal Muscle Recovery Intervention With Dietary Protein in Heart Failure

Status: Recruiting
Location: See all (2) locations...
Intervention Type: Dietary supplement
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

Severe skeletal wasting and catabolic weight loss are highly common among patients with heart failure with reduced ejection fraction (HFrEF). This prospective randomized controlled trial will compare changes in the muscle mass in the arms and the legs (appendicular lean mass) in patients with HFrEF randomized between 3 groups of no, low- or high-dose protein supplementation. The dietary protein supplementation will be Ensure(R) products manufactured by Abbott Nutrition. The Investigators hypothesize that skeletal muscle wasting in HFrEF is promoted by neurohumoral activation of catabolic metabolism (such as GDF-15 and ActRII pathways) and can be at least partially reversed by increased dietary protein intake. It is anticipated that this study will determine whether dietary protein supplementation helps to prevent muscle wasting and will advance understanding of the GDF-15 and ActRII muscle wasting pathways.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 100
Healthy Volunteers: f
View:

• Left ventricular ejection fraction (LVEF) ≤40%, New York Heart Association (NHYA) class II to IV symptoms or N-terminal pro B-natriuretic peptide (NT-proBNP) \>300 pg/mL

• Age 18 years to 100 years, inclusive

• Receiving guideline-directed medical therapy (GDMT), unless contraindicated or not tolerated

• Any of the following markers of severe HF within prior 12 months: i) Inotropic therapy; ii) 1 or more HF hospitalizations; iii) LVEF ≤25%; iv) Peak oxygen consumption (VO2) \<50% predicted or ≤16 mL/kg/min; v) 6-minute walk distance \<300 meters; vi) Unintentional weight loss \>5% of bodyweight over the past year; vii) Moderate or severe muscle wasting on physical examination; viii) NT-proBNP ≥900 pg/mL

Locations
United States
Massachusetts
Tufts Medical Center
RECRUITING
Boston
Ohio
Cleveland Clinic
RECRUITING
Cleveland
Contact Information
Primary
Amanda R Vest, MBBS
vesta2@ccf.org
2164446798
Time Frame
Start Date: 2023-04-24
Estimated Completion Date: 2027-12-31
Participants
Target number of participants: 120
Treatments
Experimental: Experimental arm
30 g/day protein supplementation (1 Ensure Max Protein® bottle)
Active_comparator: Sham comparator arm
9 g/day protein supplementation (1 Ensure Original® bottle)
No_intervention: No intervention arm
0 g/day protein supplementation (no Ensure bottles)
Related Therapeutic Areas
Sponsors
Collaborators: National Heart, Lung, and Blood Institute (NHLBI)
Leads: Tufts Medical Center

This content was sourced from clinicaltrials.gov