Safety and Efficacy of High Protein Diet Versus GFR Based Protein Diet in Heart Failure Patients With Renal Insufficiency (GFR)
Primary Purpose
Heart Failure With Reduced Ejection Fraction, Renal Insufficiency
Status
Unknown status
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
protein intake
Sponsored by
About this trial
This is an interventional treatment trial for Heart Failure With Reduced Ejection Fraction
Eligibility Criteria
Inclusion Criteria:
- Advanced HF patients class III in New York Heart Association (NYHA) based on European Society of Cardiology (ESC) definition
- Hand grip strength less than normal for age,
- Age >18 years,
- Glomerular filtration rate (GFR) 30-90,
- BMI <30, muscle mass >2 standard deviations (SDs) below mean in individuals aged 18-39 y in the NHANES III cohort.
Exclusion Criteria:
- Respiratory failure,
- Ventilator dependence,
- Dialysis treatment, and sepsis,
- Open abdominal surgery within 6 weeks prior to enrolment,
- Diseases or conditions that might change the calorie and macronutrients requirement.
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
high protein intake
GFR based protein intake
Arm Description
Study participants will receive high protein diet as recommended to preserve muscle mass (1.2-1.5 g/kg Ideal Body Weight)
Study participants will receive GFR based protein diet to preserve renal function.
Outcomes
Primary Outcome Measures
Change from baseline muscle mass at 6 months
muscle mass will be assessed by Dual-Energy X-Ray Absorptiometry (DEXA)
Secondary Outcome Measures
Change from baseline depression status at 6 months
Cardiac Depression Scale (CDS) questionnaire
Change from baseline appetite status at 6 months
Simplified Nutritional Appetite Questionnaire (SNAQ)
Change from baseline quality of life status at 6 months
Kansas City Cardiomyopathy Questionnaire
Mortality rate
Mortality occurrence
Rehospitalization
Frequency of hospital admission in 1 year
Change from baseline kidney function at 6 months
Glomerular filtration rate (GFR) (WIZARD® Automatic Gamma Counter) will be performed
Change from baseline handgrip strength at 6 months
Handgrip strength will be measured using hand grip dynamometer
Change from baseline physical performance at 6 months
SPPB score will be measured for physical performance assessment which includes: gait speed (timed 4-metre walk), sit-to-stand time (timed test of five chair rises), and standing balance (side-by-side stand, tandem and semi-tandem positions)
Full Information
NCT ID
NCT03213821
First Posted
May 8, 2017
Last Updated
July 10, 2017
Sponsor
Rajaie Cardiovascular Medical and Research Center
1. Study Identification
Unique Protocol Identification Number
NCT03213821
Brief Title
Safety and Efficacy of High Protein Diet Versus GFR Based Protein Diet in Heart Failure Patients With Renal Insufficiency
Acronym
GFR
Official Title
Safety and Efficacy of High Protein Diet Versus Glomerular Filtration Rate (GFR) Based Protein Diet in Non-obese Advanced Heart Failure (HF) Patients With Renal Insufficiency: Randomized Controlled Trial
Study Type
Interventional
2. Study Status
Record Verification Date
July 2017
Overall Recruitment Status
Unknown status
Study Start Date
November 1, 2017 (Anticipated)
Primary Completion Date
November 30, 2019 (Anticipated)
Study Completion Date
December 30, 2019 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Rajaie Cardiovascular Medical and Research Center
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Effect of high calorie high protein diet versus high calorie,glomerular filtration rate (GFR) based protein intake in non-obese advanced HF patients will be assessed. In this regard, protein intake impact will be measured on muscle mass, physical performance and renal function as main outcome. Rehospitalization, quality of life, depression an inflammatory status are second endpoints.
Detailed Description
Patient examinations:
Baseline data will be gathered on demographic and clinical characteristics, medical history, treatments and medications. Before initiating intervention, individuals will be assessed for anemia and 25 (OH) D2 and electrolytes status. Any insufficiency or imbalance will be corrected by drug therapy or supplementation. At baseline and at all visits, half or one month intervals, routine laboratory tests for heart failure patients (including Complete blood count (CBC), electrolytes status, glucose, albumin, cholesterol, triglyceride, blood urea nitrogen (BUN), C-reactive Protein (CRP),creatinine, uric acid, ferritin, 25 (OH) D, B-type natriuretic peptide (BNP), thyroid function, Prealbumin, urine analysis), appetite status and anthropometric measurements (weight, Hip and waist circumference) will be performed. At baseline and by the end of month 6, body composition, muscle mass, hand grip strength, Short Physical Performance Battery (SPPB), plasma lactate and interleukin 6 (IL-6), GFR, depression status and quality of life will be assessed. Follow up duration will be one year for measuring readmission and mortality rate. If a study participant did not attend a visit, a staff of randomized clinical trial (RCT) center will attempt to reach her/him, her/his designated friend or family member by phone call.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Heart Failure With Reduced Ejection Fraction, Renal Insufficiency
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Study design A randomized, parallel-arm, controlled pilot study is designed. Sample size is determined 50 participants per treatment arm using the stepped rules of thumb, with standardized effect sizes of 0.1 or less and power 80% for main trial (n=100). After baseline assessments, balanced permuted block method will be used for randomization. Concealment of the randomization sequence will be performed by the RCT center of Rajaie Cardiovascular, Medical and Research Center. Intervention will be according to the randomization sequence.
Masking
ParticipantCare ProviderOutcomes Assessor
Allocation
Randomized
Enrollment
100 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
high protein intake
Arm Type
Experimental
Arm Description
Study participants will receive high protein diet as recommended to preserve muscle mass (1.2-1.5 g/kg Ideal Body Weight)
Arm Title
GFR based protein intake
Arm Type
Active Comparator
Arm Description
Study participants will receive GFR based protein diet to preserve renal function.
Intervention Type
Other
Intervention Name(s)
protein intake
Intervention Description
For each participant, weighed food records of 3 consecutive days will be analyzed for estimation of calorie and macronutrient intake and dietary preferences. To make sure good compliance, diets will be developed regarding patient's dietary habits and preferences individually. High calorie (30-35 kcal/kg Ideal body weight) diets including 6-8 small meals will be formulated. Intervention group will receive high protein diet as recommended to preserve muscle mass (1.2-1.5 g/kg IBW). Comparison group will receive protein based on GFR to preserve renal function. For older adults (>65 years) protein content of diet will be as recommended by the international study group to review dietary protein needs with aging (PROT-AGE). In subjects with lower intake of protein, carbohydrate will be substituted. Both group will receive low fat diet.
Primary Outcome Measure Information:
Title
Change from baseline muscle mass at 6 months
Description
muscle mass will be assessed by Dual-Energy X-Ray Absorptiometry (DEXA)
Time Frame
At baseline and after 6 months
Secondary Outcome Measure Information:
Title
Change from baseline depression status at 6 months
Description
Cardiac Depression Scale (CDS) questionnaire
Time Frame
At Baseline and after 6 months
Title
Change from baseline appetite status at 6 months
Description
Simplified Nutritional Appetite Questionnaire (SNAQ)
Time Frame
At baseline, in each visit up to 6 months
Title
Change from baseline quality of life status at 6 months
Description
Kansas City Cardiomyopathy Questionnaire
Time Frame
AT baseline and after 6 months
Title
Mortality rate
Description
Mortality occurrence
Time Frame
Up to 1 year
Title
Rehospitalization
Description
Frequency of hospital admission in 1 year
Time Frame
Number of hospital admission will be recorded from date of intervention initiation until 1 year
Title
Change from baseline kidney function at 6 months
Description
Glomerular filtration rate (GFR) (WIZARD® Automatic Gamma Counter) will be performed
Time Frame
At baseline and after 6 months
Title
Change from baseline handgrip strength at 6 months
Description
Handgrip strength will be measured using hand grip dynamometer
Time Frame
At baseline and after 6 months
Title
Change from baseline physical performance at 6 months
Description
SPPB score will be measured for physical performance assessment which includes: gait speed (timed 4-metre walk), sit-to-stand time (timed test of five chair rises), and standing balance (side-by-side stand, tandem and semi-tandem positions)
Time Frame
At baseline and after 6 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Advanced HF patients class III in New York Heart Association (NYHA) based on European Society of Cardiology (ESC) definition
Hand grip strength less than normal for age,
Age >18 years,
Glomerular filtration rate (GFR) 30-90,
BMI <30, muscle mass >2 standard deviations (SDs) below mean in individuals aged 18-39 y in the NHANES III cohort.
Exclusion Criteria:
Respiratory failure,
Ventilator dependence,
Dialysis treatment, and sepsis,
Open abdominal surgery within 6 weeks prior to enrolment,
Diseases or conditions that might change the calorie and macronutrients requirement.
12. IPD Sharing Statement
Plan to Share IPD
No
IPD Sharing Plan Description
Data will be kept confidential.
Learn more about this trial
Safety and Efficacy of High Protein Diet Versus GFR Based Protein Diet in Heart Failure Patients With Renal Insufficiency
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