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Study of Dietary Phosphate and Mineral Homeostasis in Early Chronic Kidney Disease

Primary Purpose

Kidney Diseases

Status
Completed
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
High/ Low Phosphate diet
High/ Low Phosphate diet
High/ Low Phosphate diet
Sponsored by
University of British Columbia
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Kidney Diseases focused on measuring Chronic Kidney Disease, CKD, Diet, Dietary Phosphate, Mineral Metabolism, FGF-23

Eligibility Criteria

19 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • CKD patients with CKD stage 3 and 4 (eGFR < 60 ml/min and > 15 ml/min per 1.73 m2, not requiring dialysis).
  • Normal serum phosphate stable over three months (> 0.87 mmol/L and < 1.70 mmol/L)
  • Not yet following a low phosphate diet as reported by the patient or the renal dietitian (<1500mg/d)
  • Over 19 years of age

Exclusion Criteria:

  • Body mass index <20 kg/m2
  • Current use of phosphate binders or active vitamin D or phenytonin (which induces vitamin D catabolism)
  • Primary parathyroid defects
  • Diagnosed osteoporosis
  • Gut absorption defects
  • Liver disease
  • Pregnancy or lactation
  • Patients hospitalised within the last 4 weeks

Sites / Locations

  • St. Paul's Hospital

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Active Comparator

Active Comparator

Active Comparator

Arm Label

1

2

3

Arm Description

High/ Low Phosphate diet I. A five-day low phosphate diet / A five-day low phosphate diet with the addition of a phosphate binder / A five-day high phosphate diet. II. A five-day low phosphate diet / A five-day high phosphate diet / A five-day low phosphate diet with the addition of a phosphate binder III. A five-day high phosphate diet / A five-day low phosphate diet with the addition of a phosphate binder / A five-day low phosphate diet. IV. A five-day high phosphate diet / A five-day low phosphate diet / A five-day low phosphate diet with the addition of a phosphate binder. V. A five-day low phosphate diet with the addition of a phosphate binder / A five-day low phosphate diet / A five-day high phosphate diet. VI. A five-day low phosphate diet with the addition of a phosphate binder / A five-day high phosphate diet / A five-day low phosphate diet.

High/ Low Phosphate diet

High/ Low Phosphate diet

Outcomes

Primary Outcome Measures

FGF-23

Secondary Outcome Measures

Serum calcium, phosphate, PTH, 25 and 1,25 vitamin D and fractional phosphate excretion.

Full Information

First Posted
September 17, 2008
Last Updated
February 17, 2014
Sponsor
University of British Columbia
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1. Study Identification

Unique Protocol Identification Number
NCT00755690
Brief Title
Study of Dietary Phosphate and Mineral Homeostasis in Early Chronic Kidney Disease
Official Title
Study of Dietary Phosphate and Mineral Homeostasis in Early Chronic Kidney Disease
Study Type
Interventional

2. Study Status

Record Verification Date
February 2014
Overall Recruitment Status
Completed
Study Start Date
September 2008 (undefined)
Primary Completion Date
March 2010 (Actual)
Study Completion Date
March 2010 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of British Columbia

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
This study is designed to describe the physiological response to increased and decreased dietary phosphate intake on various parameters of mineral metabolism in the blood and urine of individuals with Chronic Kidney Disease stage 3 and 4 with normal serum phosphate levels. This detailed study will give us a far greater understanding of the role of diet in abnormal mineral homeostasis early in the progression of this chronic disease. The findings of this study will help both physicians and dietitians better determine the optimal time to introduce dietary therapy in CKD.
Detailed Description
The potential benefits of implementation of phosphate management earlier in CKD (Stages 3/4) are threefold: 1) prevention of vascular damage early in the progression of CKD thus reducing risk of cardiovascular death 2) Improved management of renal bone disease and resultant co-morbidities and 3) slowing the progression of renal failure lengthening the time required till dialysis is required. Although dietary counseling is currently a normal part of CKD care, the utility and effectiveness of lowering phosphate has not previously been quantified. In part this is due to the difficulty of measurement of serum phosphate as it is so tightly controlled before GFR falls below 30mls/min. No studies have investigated whether is it possible to modulate circulating FGF-23 and phosphate excretion in early stages of renal failure using diet in individuals with normal serum phosphate levels. Study Objectives ; To measure FGF-23 levels before and after a high phosphate diet, low phosphate diet and a low phosphate diet with phosphate binders. To measure levels of calcium, phosphate, PTH, 25 and 1,25 vitamin D and fractional phosphate excretion before and after a high phosphate diet, low phosphate diet and a low phosphate diet with phosphate binders.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Kidney Diseases
Keywords
Chronic Kidney Disease, CKD, Diet, Dietary Phosphate, Mineral Metabolism, FGF-23

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
32 (Actual)

8. Arms, Groups, and Interventions

Arm Title
1
Arm Type
Active Comparator
Arm Description
High/ Low Phosphate diet I. A five-day low phosphate diet / A five-day low phosphate diet with the addition of a phosphate binder / A five-day high phosphate diet. II. A five-day low phosphate diet / A five-day high phosphate diet / A five-day low phosphate diet with the addition of a phosphate binder III. A five-day high phosphate diet / A five-day low phosphate diet with the addition of a phosphate binder / A five-day low phosphate diet. IV. A five-day high phosphate diet / A five-day low phosphate diet / A five-day low phosphate diet with the addition of a phosphate binder. V. A five-day low phosphate diet with the addition of a phosphate binder / A five-day low phosphate diet / A five-day high phosphate diet. VI. A five-day low phosphate diet with the addition of a phosphate binder / A five-day high phosphate diet / A five-day low phosphate diet.
Arm Title
2
Arm Type
Active Comparator
Arm Description
High/ Low Phosphate diet
Arm Title
3
Arm Type
Active Comparator
Arm Description
High/ Low Phosphate diet
Intervention Type
Behavioral
Intervention Name(s)
High/ Low Phosphate diet
Intervention Description
Low phosphate diet (750mg/day).
Intervention Type
Behavioral
Intervention Name(s)
High/ Low Phosphate diet
Intervention Description
Low phosphate diet (750mg/day) with the addition of the phosphate binder aluminum hydroxide (500mg three times per day).
Intervention Type
Behavioral
Intervention Name(s)
High/ Low Phosphate diet
Intervention Description
III. High phosphate diet (2000mg /day).
Primary Outcome Measure Information:
Title
FGF-23
Time Frame
5 days
Secondary Outcome Measure Information:
Title
Serum calcium, phosphate, PTH, 25 and 1,25 vitamin D and fractional phosphate excretion.
Time Frame
5 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
19 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: CKD patients with CKD stage 3 and 4 (eGFR < 60 ml/min and > 15 ml/min per 1.73 m2, not requiring dialysis). Normal serum phosphate stable over three months (> 0.87 mmol/L and < 1.70 mmol/L) Not yet following a low phosphate diet as reported by the patient or the renal dietitian (<1500mg/d) Over 19 years of age Exclusion Criteria: Body mass index <20 kg/m2 Current use of phosphate binders or active vitamin D or phenytonin (which induces vitamin D catabolism) Primary parathyroid defects Diagnosed osteoporosis Gut absorption defects Liver disease Pregnancy or lactation Patients hospitalised within the last 4 weeks
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Adeera Levin, MD
Organizational Affiliation
University of British Columbia
Official's Role
Principal Investigator
Facility Information:
Facility Name
St. Paul's Hospital
City
Vancouver
State/Province
British Columbia
Country
Canada

12. IPD Sharing Statement

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Study of Dietary Phosphate and Mineral Homeostasis in Early Chronic Kidney Disease

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