Heart FailureNCT06256276
Nutritional Therapy for Autonomic Dysfunction in Elderly Heart Failure Patients
A study testing Whey protein powder and L-carnitine in people with Heart Failure, run by University of Arkansas at 1 site in United States.
Trial summary
Recent studies suggest that patients with heart failure (HF) may have a reduced ability to control the tone of their blood vessels, heart rate or blood pressure in response to stress. This study will test whether 16 weeks of protein supplements can improve control of blood pressure and heart rate in HF patients. Read more about this study
- Who is it for?
- Ages 60 to 90 years, women only
- Conditions the study is for
- Heart Failure
- What is being tested?
- Whey protein powder and L-carnitine
- Type of treatment
- Pill or oral medicine
- Could I receive a placebo?
- Yes, some participants may receive a placebo
- How many people
- 21 participants
- Where
- 1 siteUnited States
- Study dates
- 26 Jul 2016to 1 Feb 2018
- Phase
- Interventional
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 60 to 90 years
- Women only
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- Mild to moderate heart failure (NYHA I, II, or III symptomology) as confirmed by study physician
Who cannot join
- Moderately-severe dementia (MoCA score)
- Active inflammatory bowel disease
- Active cancer or chemotherapy in the past year
- Self-reported allergy to whey protein
- Documented insulin-dependent diabetes mellitus, or uncontrolled diabetes with hemoglobin A1C >8.5% (collected from medical record)
- >50mg doses of metoprolol or atenolol daily or more than 12.5mg twice daily of carvedilol
Show all 11Show fewer
- History of renal failure stage IV or V
- History of severe orthostasis (>20mm Hg drop in systolic pressure)
- History of high grade second degree heart block
- History of arrhythmias (atrial or ventricular, tachy or brady)
- Other criteria as determined by the study physician
Trial locations and contacts
1 site in 1 country.
United States1 site
University of Arkansas for Medical Sciences
Little Rock, Arkansas, 72205
About this study
Recent studies suggest that patients with heart failure (HF) may have a reduced ability to control the tone of their blood vessels, heart rate or blood pressure in response to stress. This study will test whether 16 weeks of protein supplements can improve control of blood pressure and heart rate in HF patients.
Read the detailed description
Heart Failure is defined as "a complex clinical syndrome that can result from any structural or functional cardiac disorder that impairs the ability of the ventricle to fill or eject blood." The New York Heart Association classifies heart failure four functional classes: NYHA 1-4, with Class 1 as minimal and Class 4 as the most advanced stage.
As a clinical syndrome, HF can be associated with significant limitations in functional capacity which can be very debilitating in the elderly population. It is a major cause of morbidity and mortality and is the leading cause of hospitalization among older individuals in the United States (1-15), particularly among those aged ≥65 years (16, 18). Nearly 1 million hospitalizations for HF occur each year with rates of hospitalization continuing to rise. Prevalence of heart failure was estimated to be more than 5.8 million in the United States and HF was singled out as an emerging epidemic (17).
Heart failure is associated with autonomic and endothelial dysfunction. Recent studies suggest that patients with HF maybe more prone to having impaired vasomotor and autonomic response to stress (19-29). A reduced ability to increase blood flow or heart rate appropriately in response to demand could limit the functional capacity of these subjects and would contribute to orthostasis (drop in blood pressure on standing). Another factor contributing to orthostasis in these individuals is poor muscle tone in the lower extremities reducing venous flow.
Endothelial dysfunction in HF on the other hand is attributed to decreased production of NO and increased oxidative stress due to neurohumoral activation, release of inflammatory messengers from the myocardium, altered local shear force and resultant atherogenesis (30, 31). The endothelial dysfunction itself causes an increase in the production of cytokines, uncoupling of eNOS and further increases the oxidative stress (32-35). The endothelium helps in regulating the vascular tone by balancing the production of vasodilators and vasoconstrictors in response to various stimuli (36) and its dysfunction would also impair baroreceptor function which in turn would affect cardiac autonomic activity and blood flow.
In our research we hope to improve both autonomic and endothelial function by supplementing protein and carnitine in diet. Studies have shown that when protein is metabolized to the amino acids L-arginine and citrulline, there is increased synthesis of NO (37). L-arginine, a semi-essential basic amino acid, is a precursor in the formation of nitric oxide by the enzyme nitric oxide synthase and directly increases the formation of NO (38). The administration of arginine and/or citrulline in patients in HF has been reported to improve endothelial function. Systolic and diastolic arterial pressures as well as pulmonary arterial systolic pressure have been shown to decrease significantly after administration of arginine or citrulline administration, which in turn improves right ventricular diastolic diameter (37, 39). One clinical study reported improvement in pulmonary artery pressure and right ventricular ejection fraction after two months of oral supplementation with L-arginine or citrulline in patients with HF and right ventricular dysfunction (39). It is hoped that protein supplementation will improve autonomic function by having a positive impact on physiological and biochemical parameters, including nitric oxide synthesis which is expect will improve baroreceptor blood flow, autonomic BP and HR in response to tilt.
Carnitine supplementation of 1g/d for 12 wk in hemodialysis patients significantly reduced systemic inflammation, as reflected by decreases in CRP, IL-1β, and IL-6 (40). In obesity, the mitochondrial abnormalities of reduced fatty acid oxidation, incomplete β-oxidation, and impaired substrate switching from fatty acid to pyruvate were reversed after 8wks of oral supplementation with the same dosage of carnitine (41). It is anticipated the same beneficial effects of carnitine in individuals with HF.
The purpose of this study is to evaluate the effects of 16 weeks of protein supplementation on measures of autonomic regulation of blood pressure and heart rate, as well as physical strength and function in elderly subjects with mild to moderate heart failure (NYHA 1, 2, or 3). Each participant will be randomized to one of two groups (whey protein + L-carnitine or placebos). Study endpoints will be measured at baseline and after 4 months of treatment.
- Conditions
- Heart Failure
- Being tested
- Whey protein powder and L-carnitine, Maltodextrin placebo powder and Psyllium Husk capsules
- Medical subject headings
- Heart Failure
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Whey protein powder and L-carnitineDietary supplement
Also called Dymatize Elite Whey, Europa Sports Products
Dietary supplement intervention for 16 weeks
Maltodextrin placebo powder and Psyllium Husk capsulesDietary supplement
Maltodextrin placebo powder and Psyllium Husk capsules
| Study group | Role | What they receive |
|---|---|---|
| Whey protein powder and L-carnitine capsules | Experimental | Subjects will daily consume whey protein powder to supplement normal daily protein intake up to 1.2g protein/kg body weight per day (1 or 2 scoops powder), as well as 2 capsules (1 gram) L-carnitine for 16 weeks. Receives: Dietary Supplement: Whey protein powder and L-carnitine |
| Maltodextrin placebo powder and Psyllium Husk capsules | Placebo comparator | Subjects will daily consume maltodextrin powder as if to supplement normal daily protein intake up to 1.2g protein/kg body weight per day (1 or 2 scoops powder), as well as 2 capsules (1 gram) psyllium husk for 16 weeks. Receives: Dietary Supplement: Maltodextrin placebo powder and Psyllium Husk capsules |
What is being measured
The primary outcome is the main question the study is designed to answer.
Cardiovascular assessment of blood pressure
Measuring orthostatic blood pressure
Measured: Change from baseline to 16 weeks
Cardiovascular assessment
Measuring heart rate before and after intervention
Measured: Change from baseline to 16 weeks
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted13 Feb 2024
- Study start26 Jul 2016
- Primary completion11 Jan 2018
- Study completion1 Feb 2018
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Heart FailureStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Basic science
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Triple blind
- Who is masked
- Participant, Investigator, Outcomes assessor
- Enrolment
- 21 participants (actual)
Sponsor and investigators
- Lead sponsor
- University of Arkansas
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
- Investigators
- Gohar Azhar, M.D., Principal investigator, University of Arkansas
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06256276
- Sponsor's protocol ID
- 202617
- Status last verified
- Jan 2024
- First submitted
- 2 Feb 2024
- Last updated
- 13 Feb 2024
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 13 Feb 2024. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Nutritional Therapy for Autonomic Dysfunction in Elderly Heart Failure Patients
- ClinicalTrials.gov ID
- NCT06256276
- Acronym / sponsor ID
- 202617
- Conditions
- Heart Failure
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 21 participants (actual)
- Lead sponsor
- University of ArkansasUniversity, hospital or other
- Study start
- 26 Jul 2016 (actual)
- Primary completion
- 11 Jan 2018 (actual)
- Study completion
- 1 Feb 2018 (actual)
- First posted
- 13 Feb 2024 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Recent studies suggest that patients with heart failure (HF) may have a reduced ability to control the tone of their blood vessels, heart rate or blood pressure in response to stress. This study will test whether 16 weeks of protein supplements can improve control of blood pressure and heart rate in HF patients.
Detailed description
Heart Failure is defined as "a complex clinical syndrome that can result from any structural or functional cardiac disorder that impairs the ability of the ventricle to fill or eject blood." The New York Heart Association classifies heart failure four functional classes: NYHA 1-4, with Class 1 as minimal and Class 4 as the most advanced stage.
As a clinical syndrome, HF can be associated with significant limitations in functional capacity which can be very debilitating in the elderly population. It is a major cause of morbidity and mortality and is the leading cause of hospitalization among older individuals in the United States (1-15), particularly among those aged ≥65 years (16, 18). Nearly 1 million hospitalizations for HF occur each year with rates of hospitalization continuing to rise. Prevalence of heart failure was estimated to be more than 5.8 million in the United States and HF was singled out as an emerging epidemic (17).
Heart failure is associated with autonomic and endothelial dysfunction. Recent studies suggest that patients with HF maybe more prone to having impaired vasomotor and autonomic response to stress (19-29). A reduced ability to increase blood flow or heart rate appropriately in response to demand could limit the functional capacity of these subjects and would contribute to orthostasis (drop in blood pressure on standing). Another factor contributing to orthostasis in these individuals is poor muscle tone in the lower extremities reducing venous flow.
Endothelial dysfunction in HF on the other hand is attributed to decreased production of NO and increased oxidative stress due to neurohumoral activation, release of inflammatory messengers from the myocardium, altered local shear force and resultant atherogenesis (30, 31). The endothelial dysfunction itself causes an increase in the production of cytokines, uncoupling of eNOS and further increases the oxidative stress (32-35). The endothelium helps in regulating the vascular tone by balancing the production of vasodilators and vasoconstrictors in response to various stimuli (36) and its dysfunction would also impair baroreceptor function which in turn would affect cardiac autonomic activity and blood flow.
In our research we hope to improve both autonomic and endothelial function by supplementing protein and carnitine in diet. Studies have shown that when protein is metabolized to the amino acids L-arginine and citrulline, there is increased synthesis of NO (37). L-arginine, a semi-essential basic amino acid, is a precursor in the formation of nitric oxide by the enzyme nitric oxide synthase and directly increases the formation of NO (38). The administration of arginine and/or citrulline in patients in HF has been reported to improve endothelial function. Systolic and diastolic arterial pressures as well as pulmonary arterial systolic pressure have been shown to decrease significantly after administration of arginine or citrulline administration, which in turn improves right ventricular diastolic diameter (37, 39). One clinical study reported improvement in pulmonary artery pressure and right ventricular ejection fraction after two months of oral supplementation with L-arginine or citrulline in patients with HF and right ventricular dysfunction (39). It is hoped that protein supplementation will improve autonomic function by having a positive impact on physiological and biochemical parameters, including nitric oxide synthesis which is expect will improve baroreceptor blood flow, autonomic BP and HR in response to tilt.
Carnitine supplementation of 1g/d for 12 wk in hemodialysis patients significantly reduced systemic inflammation, as reflected by decreases in CRP, IL-1β, and IL-6 (40). In obesity, the mitochondrial abnormalities of reduced fatty acid oxidation, incomplete β-oxidation, and impaired substrate switching from fatty acid to pyruvate were reversed after 8wks of oral supplementation with the same dosage of carnitine (41). It is anticipated the same beneficial effects of carnitine in individuals with HF.
The purpose of this study is to evaluate the effects of 16 weeks of protein supplementation on measures of autonomic regulation of blood pressure and heart rate, as well as physical strength and function in elderly subjects with mild to moderate heart failure (NYHA 1, 2, or 3). Each participant will be randomized to one of two groups (whey protein + L-carnitine or placebos). Study endpoints will be measured at baseline and after 4 months of treatment.
Study design
- Primary purpose
- Basic science
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Triple blind (participant, investigator, outcomes assessor)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Whey protein powder and L-carnitine capsules | Experimental | Dietary Supplement: Whey protein powder and L-carnitineSubjects will daily consume whey protein powder to supplement normal daily protein intake up to 1.2g protein/kg body weight per day (1 or 2 scoops powder), as well as 2 capsules (1 gram) L-carnitine for 16 weeks. |
| Maltodextrin placebo powder and Psyllium Husk capsules | Placebo comparator | Dietary Supplement: Maltodextrin placebo powder and Psyllium Husk capsulesSubjects will daily consume maltodextrin powder as if to supplement normal daily protein intake up to 1.2g protein/kg body weight per day (1 or 2 scoops powder), as well as 2 capsules (1 gram) psyllium husk for 16 weeks. |
Who may qualify
- Ages
- 60 to 90 years
- Sex
- Female only
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (1 listed)
- Mild to moderate heart failure (NYHA I, II, or III symptomology) as confirmed by study physician
Key exclusion criteria (11 listed)
- Moderately-severe dementia (MoCA score)
- Active inflammatory bowel disease
- Active cancer or chemotherapy in the past year
- Self-reported allergy to whey protein
- Documented insulin-dependent diabetes mellitus, or uncontrolled diabetes with hemoglobin A1C >8.5% (collected from medical record)
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Whey protein powder and L-carnitineAlso: Dymatize Elite Whey, Europa Sports ProductsDietary supplement intervention for 16 weeks | Dietary supplement | Whey protein powder and L-carnitine capsules |
| Maltodextrin placebo powder and Psyllium Husk capsulesMaltodextrin placebo powder and Psyllium Husk capsules | Dietary supplement | Maltodextrin placebo powder and Psyllium Husk capsules |
Primary outcome
Cardiovascular assessment of blood pressure
Time frame: Change from baseline to 16 weeks
Measuring orthostatic blood pressure
Cardiovascular assessment
Time frame: Change from baseline to 16 weeks
Measuring heart rate before and after intervention
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 13 Feb 2024.
- Individual participant dataSharing planned: No
Related trials for Heart Failure
RecruitingPhase 3
Maridebart Cafraglutide in Heart Failure With Preserved or Mildly Reduced Ejection Fraction and Obesity
Heart Failure With Preserved Ejection Fraction, Heart Failure With Mildly Reduced Ejection Fraction
Recruiting
Evaluation of the Effects of Sauna Therapy on Congestion and Loop Diuretic Use in Patients With Heart Failure With Reduced or Moderately Reduced Ejection Fraction
Heart Failure
Recruiting
PrEcision Pacing in HFpEF: the PEP-HFpEF Trial
Heart Failure and Preserved Ejection Fraction, Heart Failure New York Heart Association Class III
Enrolling by invitation
EXCOR Active Driving System for the EXCOR Pediatric VAD IDE Study
Heart Failure, Transplant; Failure, Heart
Enrolling by invitationObservational study
Multi-Scale Analysis of Phenotypes in Heart Failure (MAP-HEART)
Heart Failure
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Gohar Azhar, M.D. principal investigator
University of Arkansas
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Whey protein powder and L-carnitine in people with Heart Failure, run by University of Arkansas at 1 site in United States.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 1 inclusion and 11 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 13 Feb 2024. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Cardiovascular assessment of blood pressure (time frame: Change from baseline to 16 weeks). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 13 Feb 2024.