- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04942548
Reverse HFpEF: Ketogenic Reversal of Heart Failure With Preserved Ejection Fraction Study
Study Overview
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Colorado
-
Denver, Colorado, United States, 80206
- National Jewish Health and University of Colorado Denver
-
Denver, Colorado, United States, 80218
- Saint Joseph Hospital
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Adults (age 21-80) who meet clinical signs and symptoms of heart failure based on clinical assessment.
- The subject must meet at least one of the following hemodynamic criteria for HFpEF of PH-HFpEF by right heart catheterization (RHC) within 6 months of screening visit;
A) HFpEF:
- At rest: mean pulmonary artery occlusions pressure (PAOP) > 15, pulmonary vascular resistance (PVR) < 3 Wood Units, or
- HFpEF with fluid challenge, defined as increase in PAOP post 500 cc fluid bolus: mean PAOP > 18, PVR < 3 Wood Units, or
- HFpEF with exercise, defined as peak mean PAOP > 17, PVR < 3 Wood Units if age < 50 or peak mean PAOP > 19 and PVR < 3 Wood Units if age >= 50
B) PH-HFpEF:
- At rest: mean pulmonary artery occlusion pressure (PAOP) > 15, mean pulmonary artery pressure (PAP) >= 25, pulmonary vascular resistance (PVR) > 3 Wood Units, or
- PH-HFpEF with fluid challenge, defined as increase in PAOP post 500 cc fluid bolus: mean PAOP > 18, mean PAP >= 25, PVR > 3 Wood Units, or
PH-HFpEF with exercise, defined as peak mean PAOP > 17, peak mean PAP > 30, peak PVR > 1.34 Wood Units if age < 50 or peak mean PAOP > 19, peak mean PAP > 33, and PVR < 2.1 Wood Units if age >= 50
- The subject also must meet criteria for metabolic syndrome, defined as: Abdominal obesity (BMI > 30 kg/m2 or abdominal obesity, waist circumference > 102 cm men, > 88 cm women) AND 2 of the following;
a. Currently being treated for systemic hypertension or blood pressure (BP) >= 135/85 b. Glucose intolerance with diagnosis of type 2 diabetes, or fasting blood glucose 110-125 mg/dL or hemoglobin A1c > 6% c. Triglycerides >= 150, or on treatment for high triglycerides d. HDL < 40 men, < 50 women, or on treatment for high triglycerides
- If the subject is on pulmonary hypertension specific vasodilators, they must be on stable medical therapy without changes to pulmonary vasodilator medication within 3 months prior to screening visit.
- The subject must have also had a cardiopulmonary exercise test within 6 months of screening visit.
- The subject must have also had an echocardiogram within 6 months of screening visit.
- The subject must have demonstrated stable weight (less that 5% weight loss) 3 months prior to screening visit. (They cannot already be losing weight).
- The subject owns and uses a smartphone or tablet.
- Must speak English
Exclusion Criteria:
- The subject is already on a significant weight loss trajectory prior to study entry.
- The subject cannot be on an alternative diet plan or strategy (e.g., Weight Watchers, Nutrisystem, Ornish).
- Left ventricular ejection fraction < 50%.
- Severe valvular disease by echocardiogram or dysfunctional prosthetic valve.
- Active pericardial disease (moderate or large pericardial effusion or constrictive pericarditis).
- Active coronary ischemia defined by abnormal stress test, angiogram, or coronary CT angiography per investigator.
- Prolonged corrected QT interval (QTc) > 450 ms
Significant lung disease on pulmonary function tests (PFT's) within the 6 months of screening visit, (Both post-bronchodilator values and pre-bronchodilator values must meet exclusion criteria. If either post- or pre-bronchodilator values do not, the subject may be included) defined as either:
- Irreversible obstructive airways disease (post-bronchodilator forced expiratory volume/forced vital capacity (FEV1/FVC) < 70% predicted) or
- Restrictive lung disease (FVC < 70% predicted. If total lung capacity (TLC) is >= 70%, it is acceptable to have an FVC of < 70%) or
- More than mild radiographic pulmonary disease as determine don CT scan within the past 2 years per investigator.
- History of non-adherence to diuretics within 3 months of screening visit.
- History or recurrent severe hypokalemia, potassium < 3.0 mg/dL.
- History of kidney stones, gout, or gallbladder disease unless in the opinion of the investigator it will not impact the safety of the patient
- C-peptide < 0.5 ng/mL (increased risk of diabetic ketoacidosis (DKA))
- Uncorrected anemia (hemoglobin < 10 g/dL).
- Unable to participate in the comprehensive ketogenic diet program, including biometric data acquisition and data entry (glucometer self-stick and smartphone use).
- Unable or unwilling to prepare meals for self.
- Unable to perform quantitative cardia testing regimen (cardiopulmonary exercise testing, 6-minute walk).
- Subject is pregnant or planning to become pregnant in the next 14 months.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: HFpEF
Patients diagnosed with obesity related heart failure with preserved ejection fraction(HFpEF)
|
Ketogenic diet intervention that is high in fat and low in carbohydrates, causing the body to induce a state of metabolic ketosis, whereby fat is broken down into ketones to provide an energy source for the body.
|
|
Experimental: PH-HFpEF
Patients diagnosed with obesity related pulmonary hypertension heart failure with preserved ejection fraction (PH-HFpEF)
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Ketogenic diet intervention that is high in fat and low in carbohydrates, causing the body to induce a state of metabolic ketosis, whereby fat is broken down into ketones to provide an energy source for the body.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
MLHFQ Questionnaire
Time Frame: 6 Months
|
Change in score on the Minnesota Living with Heart Failure Quality of Life (MLHFQ) Questionnaire for the HFpEF cohort.
|
6 Months
|
|
PAH-SYMPACT Questionnaire
Time Frame: 6 Months
|
Change in score on the Pulmonary Arterial Hypertension-Symptoms and Impact (PAH-SYMPACT) Questionnaire for the PH-HFpEF cohort.
|
6 Months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in Metabolic Health: Weight
Time Frame: 6 Months
|
Weight in kilograms (kg)
|
6 Months
|
|
Change in Metabolic Health: Glucose
Time Frame: 6 Months
|
Glucose in milligrams per deciliter (mg/dL)
|
6 Months
|
|
Change in Metabolic Health: Insulin
Time Frame: 6 Months
|
Insulin in microinternational unit per milliliter (uIU/mL)
|
6 Months
|
|
Change in Metabolic Health: Homeostatic Model Assessment for Insulin Resistance (HOMA-IR)
Time Frame: 6 Months
|
Insulin and glucose are multiplied then divided by 405 to report HOMA-IR
|
6 Months
|
|
Change in Metabolic Health: Albumin
Time Frame: 6 Months
|
Albumin in grams per deciliter (g/dL)
|
6 Months
|
|
Change in Metabolic Health: Bilirubin total
Time Frame: 6 Months
|
Bilirubin total in milligrams per deciliter (mg/dL)
|
6 Months
|
|
Change in Metabolic Health: Alanine Transaminase (ALT)
Time Frame: 6 Months
|
ALT in units per liter (U/L)
|
6 Months
|
|
Change in Metabolic Health: Aspartate Aminotransferase (AST)
Time Frame: 6 Months
|
AST in units per liter (U/L)
|
6 Months
|
|
Change in Metabolic Health: Alkaline Phosphatase (ALP)
Time Frame: 6 Months
|
ALP in units per liter (U/L)
|
6 Months
|
|
Change in Metabolic Health: High Sensitivity C-Reactive Protein (HS-CRP)
Time Frame: 6 Months
|
HS-CRP in milligrams per deciliter (mg/dL)
|
6 Months
|
|
Change in Metabolic Health: Triglycerides
Time Frame: 6 Months
|
triglyceride in milligrams per deciliter (mg/dL)
|
6 Months
|
|
Change in Metabolic Health: High Density Lipoprotein (HDL)
Time Frame: 6 Months
|
HDL in milligrams per deciliter (mg/dL)
|
6 Months
|
|
Change in Metabolic Health: Hemoglobin A1c
Time Frame: 6 Months
|
hemoglobin A1c in percent (%)
|
6 Months
|
|
Change in Metabolic Health: Body Mass Index (BMI)
Time Frame: 6 Months
|
Weight and height will be combined to report BMI in kg/m^2
|
6 Months
|
|
Changes in Physical Function: 6 Minute Walk Test (6MWT)
Time Frame: 6 Months
|
6-minute walk test is reported in meters (m) of how far a subject walks in 6 minutes
|
6 Months
|
|
Changes in Physical Function: Maximum Oxygen Consumption (VO2max)
Time Frame: 6 Months
|
VO2 max is reported in liters per minute (L/min) while performing a cardiopulmonary exercise test (CPET)
|
6 Months
|
|
Changes in Physical Function: Maximum Work
Time Frame: 6 Months
|
Maximum work achieved while performing a cardiopulmonary exercise test (CPET) is reported in watts (W)
|
6 Months
|
|
Changes in Physical Function: 30 Second Sit-to-Stand test (30s STS)
Time Frame: 6 Months
|
30s STS is reported in quantity of how many times the subject can come to a full stand from a seated position in 30 seconds (s)
|
6 Months
|
|
Changes in Physical Function: Leg Press - 1 Repetition Maximum
Time Frame: 6 Months
|
Leg press is reported in kilograms (kg)
|
6 Months
|
|
Changes in Physical Function: Chest Press - 1 Repetition Maximum
Time Frame: 6 Months
|
Chest press is reported in kilograms (kg)
|
6 Months
|
|
Changes in Physical Function: Leg Extension - 1 Repetition Maximum
Time Frame: 6 Months
|
Leg extension is reported in kilograms (kg)
|
6 Months
|
|
Cardiac Remodeling: Changes in the Left Ventricle (LV) size
Time Frame: 6 Months
|
This is determined by the internal diameter measurement of the LV, reported in centimeters (cm) from a subject performed echocardiogram
|
6 Months
|
|
Cardiac Remodeling: Changes in the Left Ventricle (LV) thickness
Time Frame: 6 Months
|
This is determined by a measurement of the LV wall, reported in millimeters (mm) from an echocardiogram.
|
6 Months
|
|
Cardiac Remodeling: Changes in the Left Ventricle (LV) mass
Time Frame: 6 Months
|
This is determined by a combination formula of the interventricular septum diastole (IVSd), left ventricle diastole (LVd), and posterior wall diastole (PWd), calculated by an echocardiogram and reported in grams (g).
|
6 Months
|
|
Cardiac Remodeling: Changes in Left Atrium (LA) size
Time Frame: 6 Months
|
This is determined by the internal diameter measurement of the LA, reported in centimeters (cm) from a subject performed echocardiogram.
|
6 Months
|
|
Cardiac Remodeling: Changes in Inferior Vena Cava (IVC) size
Time Frame: 6 Months
|
This is determined by the internal diameter perpendicular to the long axis of the IVC at the end-expiration, reported in centimeters (cm) from the echocardiogram.
|
6 Months
|
|
Cardiac Remodeling: Changes in estimated Right Atrial Pressure (RAP)
Time Frame: 6 Months
|
This is determined by a combination equation subtracting the venous return (VR) from the central venous pressure (CVP), reported in millimeters of mercury (mmHg) from the echocardiogram.
|
6 Months
|
|
Cardiac Remodeling: Changes in Right Ventricle Systolic Pressure (RVSP)
Time Frame: 6 Months
|
This estimates the pressure inside the artery that supplies the lung with blood, reported in millimeters of mercury (mmHg) from the echocardiogram.
|
6 Months
|
|
Changes in the rate of mitral annulus velocity (e')
Time Frame: 6 Months
|
e' is reported in centimeters per second (cm/s) based on a subject performed echocardiogram
|
6 Months
|
|
Changes in the ratio of transmitral early peak velocity (E) by pulsed wave Doppler over e' (E/e')
Time Frame: 6 Months
|
E/e' is reported as an integer based on the transmitral early peak velocity (E) over the mitral annulus velocity (e') from a subject performed echocardiogram.
|
6 Months
|
|
PH-HFpEF Only Hemodynamics: Changes in Right Atrial Pressure (RAP)
Time Frame: 6 Months
|
This is determined by a combination equation subtracting the venous return (VR) from the central venous pressure (CVP), reported in millimeters of mercury (mmHg) from the echocardiogram.
|
6 Months
|
|
PH-HFpEF Only Hemodynamics: Changes in Pulmonary Artery Pressure (PAP)
Time Frame: 6 Months
|
This is calculated from systolic, by Tricuspid Regurgitation maximum (TRmax) and diastolic, by Pulmonary Regurgitation-end velocity (PR-end) pulmonary artery pressures, reported in millimeters of mercury (mmHg) from the echocardiogram.
|
6 Months
|
|
PH-HFpEF Only Hemodynamics: Changes in Pulmonary Artery Occlusive Pressure (PAOP)
Time Frame: 6 Months
|
This is determined by the pressure value of the pulmonary artery once it's occluded during a Right Heart Catheterization (RHC), measured in millimeters of mercury (mmHg).
|
6 Months
|
|
PH-HFpEF Only Hemodynamics: Changes in Pulmonary Vascular Resistance (PVR)
Time Frame: 6 Months
|
Left Atrial Pressure (LAP), Pulmonary Artery Pressure (PAP) and Cardiac Output (CO) are combined to report the PVR in Wood Units (WU) from a Right Heart Catheterization (RHC).
|
6 Months
|
|
PH-HFpEF Only Hemodynamics: Changes in Cardiac Output (CO)
Time Frame: 6 Months
|
Stoke Volume (SV) and Heart Rate (HR) are combined to report CO in liters per minute (L/min) from the right heart catheterization.
|
6 Months
|
|
PH-HFpEF Only Hemodynamics: Changes in Cardiac Index (CI)
Time Frame: 6 Months
|
Cardiac Output (CO) and Body Surface Area (BSA) are combined to report CI in liters per minute per meters squared (L/min/m^2) from a Right Heart Catherization (RHC).
|
6 Months
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- HS-3243 Keto
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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