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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
Rajaie Cardiovascular Medical and Research Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Heart Failure With Reduced Ejection Fraction

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

    First Posted
    May 8, 2017
    Last Updated
    July 10, 2017
    Sponsor
    Rajaie Cardiovascular Medical and Research Center
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    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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