Evaluation of Increased Fruits and Vegetables Consumption in Chronic Kidney Disease
Primary Purpose
Chronic Kidney Diseases
Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Fruits and Vegetable increase
Sponsored by
About this trial
This is an interventional supportive care trial for Chronic Kidney Diseases
Eligibility Criteria
Inclusion Criteria:
- Adult patients ≥ 18 years of age with chronic kidney disease and hyperkalemia
- Chronic kidney disease is defined as eGFR 15-44ml/min/1.73m2
- Documented hyperkalemia which is defined as serum potassium ≥ 5.0 mmol/L during the last 90 days
- Diet evaluation for hyperkalemia (serum potassium ≥ 5.0) during the last 90 days
- Patients receiving RASS inhibitors, beta-blockers, or diuretics to be on stable doses for 2 weeks
Exclusion Criteria:
- Patients with a known allergy to patiromer
- Patients currently taking patiromer or other potassium controlling agents.
Sites / Locations
- NY HealthRecruiting
Arms of the Study
Arm 1
Arm Type
Other
Arm Label
chronic kidney disease patients
Arm Description
Evaluation of Increased fruits and vegetables consumption in chronic kidney disease patients maintaining normokalemia with patiromer
Outcomes
Primary Outcome Measures
By increasing the consumption of Fruits and Vegetable in their daily diet using the Nutritional Fruits and Vegetable Diary based off of the USDA Nutritive Value of foods and completing the Quality of Life Nutritional Questionnaire.
Participants will increase the Fruit and vegetable consumption by following a Diet plan listed in the Nutritional Diary provided to them by the study site in the beginning of the study while taking Patiromer (Veltassa). This will record their daily intake of 26-28 servings of fruit and vegetables weekly. The Nutritional diary lists a Diet Plan that measures the serving size of 26-28 servings of the fruits and vegetables. The measurement of fruits and vegetables has been calculated by the Nutritionist based off of the USDA Nutritive Value of foods and listed on the diary to explain the serving sizes and suggestions of meal plans.
Secondary Outcome Measures
The Kidney Function levels will be tested at each visit from blood samples provided by the subject.
The Kidney Function blood test samples will be taken from the subject to show overall kidney health in Chronic Kidney Disease Patients by increasing their fruit and vegetable intake while on patiromer. The blood tests that support this is , Magnesium, phosphorus, iPTH, lipid panel, uric acid, hemoglobin A1C, Vitamin D 25(OH), Vitamin D 1,25(OH), FGF-23 and CBC panel.
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT05050110
Brief Title
Evaluation of Increased Fruits and Vegetables Consumption in Chronic Kidney Disease
Official Title
Evaluation of Increased Fruits and Vegetables Consumption in Chronic Kidney Disease Patients Maintaining Normokalemia With Patiromer
Study Type
Interventional
2. Study Status
Record Verification Date
September 2022
Overall Recruitment Status
Recruiting
Study Start Date
November 24, 2020 (Actual)
Primary Completion Date
January 2024 (Anticipated)
Study Completion Date
January 2024 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Nand Wadhwa
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
This study aims to investigate the feasibility of increasing dietary consumption of a rich variety of fruits and vegetables (including those that are potassim-rich) in patients with chronic kidney disease through use of nutritional counselling and hyperkalemia management with patiromer
Detailed Description
Adult Patients ages 18 and older with a diagnosis of Chronic Kidney Disease will be given a Diet Plan that consist of an increase of Fruits and Vegetables. Baseline data will be collected after the subject has signed the consent and their most recent eGFR and potassium level that is within 90 days has been reviewed to determine they are within the inclusion criteria.
Based on the approved Veltassa package insert the subject will begin to take daily. During this control period of two weeks, the subject will document their normal daily consumption of fruits and vegetables in a provided food diary.
On the Second week, patient will receive dietary/nutritional counseling on the importance of potassium-rich fruits and vegetables. They will be instructed to increase their fruit and vegetable intake based on personal preferences and nutritional guides located inside the food diary. Choices will be documented daily in the supplied food diaries.
The Bowel Diary will be classified according to the Bristol Stool Chart and Quality of Life. Nutrition Survey Questionnaire will be documented in that supplied log.
At each subsequent visit, food diaries will be reviewed to evaluate fruit and vegetable consumption, vital signs will be documented and labs collected to measure effects on potassium metabolism. Bowel habits and questionnaires will be completed by the subject to determine how their diet has affected their quality of life.
Patiromer (Veltessa) dosing will be adjusted based on their serum potassium values following the approved drug brochure guidelines and at the discretion of the investigator.
Subject will return to the clinic at specified time points up to 52 weeks on study. The Patient can continue Veltassa while in the follow up period until week 52 at the discretion of the Principle Investigator.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Kidney Diseases
7. Study Design
Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
Evaluation of Increased fruits and vegetables consumption in chronic kidney disease patients maintaining normokalemia with patiromer
Masking
None (Open Label)
Allocation
N/A
Enrollment
40 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
chronic kidney disease patients
Arm Type
Other
Arm Description
Evaluation of Increased fruits and vegetables consumption in chronic kidney disease patients maintaining normokalemia with patiromer
Intervention Type
Other
Intervention Name(s)
Fruits and Vegetable increase
Intervention Description
Increase fruits and vegetable consumption in chronic Kidney Patients to maintain Normokalemia
Primary Outcome Measure Information:
Title
By increasing the consumption of Fruits and Vegetable in their daily diet using the Nutritional Fruits and Vegetable Diary based off of the USDA Nutritive Value of foods and completing the Quality of Life Nutritional Questionnaire.
Description
Participants will increase the Fruit and vegetable consumption by following a Diet plan listed in the Nutritional Diary provided to them by the study site in the beginning of the study while taking Patiromer (Veltassa). This will record their daily intake of 26-28 servings of fruit and vegetables weekly. The Nutritional diary lists a Diet Plan that measures the serving size of 26-28 servings of the fruits and vegetables. The measurement of fruits and vegetables has been calculated by the Nutritionist based off of the USDA Nutritive Value of foods and listed on the diary to explain the serving sizes and suggestions of meal plans.
Time Frame
3 years
Secondary Outcome Measure Information:
Title
The Kidney Function levels will be tested at each visit from blood samples provided by the subject.
Description
The Kidney Function blood test samples will be taken from the subject to show overall kidney health in Chronic Kidney Disease Patients by increasing their fruit and vegetable intake while on patiromer. The blood tests that support this is , Magnesium, phosphorus, iPTH, lipid panel, uric acid, hemoglobin A1C, Vitamin D 25(OH), Vitamin D 1,25(OH), FGF-23 and CBC panel.
Time Frame
3 years
Other Pre-specified Outcome Measures:
Title
Measure the subjects diet intake related to Quality of Life
Description
The subject will complete a Quality of Life Nutritional Questionnaire which is an instrument supported by ncbi to assess quality of life in relation to nutrition.
Time Frame
3 years
Title
Measure the description of Daily bowel moments to test for constipation
Description
Patient will complete a daily bowel Diary based on the Bristol Stool Chart which is a medical aid designed to classify feces into seven groups. The Diary will be provided to the subject to observe and classify their daily bowel movements.
Time Frame
3 years
Title
Urine will be measured to evaluate kidney function in subjects with Chronic kidney disease
Description
Tests will include 24 hour urine & Random for sodium, potassium, chloride, magnesium, phosphorus, calcium, urea nitrogen, creatinine, protein, albumin
Time Frame
3 years
Title
Measure serum Potassium blood levels to remain below 5mmol/L
Description
Serum Potassium levels are measured by blood samples from the subject that consists of either A Comprehensive Metabolic Panel blood test which includes or Basic Metabolic Panel depending on the timepoint in the study.
Time Frame
3 years
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Adult patients ≥ 18 years of age with chronic kidney disease and hyperkalemia
Chronic kidney disease is defined as eGFR 15-44ml/min/1.73m2
Documented hyperkalemia which is defined as serum potassium ≥ 5.0 mmol/L during the last 90 days
Diet evaluation for hyperkalemia (serum potassium ≥ 5.0) during the last 90 days
Patients receiving RASS inhibitors, beta-blockers, or diuretics to be on stable doses for 2 weeks
Exclusion Criteria:
Patients with a known allergy to patiromer
Patients currently taking patiromer or other potassium controlling agents.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Megan Stahl
Phone
631-675-5075
Email
mstahl@nycancer.com
First Name & Middle Initial & Last Name or Official Title & Degree
Laura Brady
Phone
631-675-5075
Email
lbrady@nycancer.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Nand Wadwha, MD
Organizational Affiliation
NY Health
Official's Role
Principal Investigator
Facility Information:
Facility Name
NY Health
City
Port Jefferson Station
State/Province
New York
ZIP/Postal Code
11776
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Megan Stahl
Phone
631-675-5075
Email
mstahl@nycancer.com
First Name & Middle Initial & Last Name & Degree
Laura Brady
Phone
631-675-5075
Email
lbrady@nycancer.com
First Name & Middle Initial & Last Name & Degree
Nand Wadwha, MD
12. IPD Sharing Statement
Learn more about this trial
Evaluation of Increased Fruits and Vegetables Consumption in Chronic Kidney Disease
We'll reach out to this number within 24 hrs