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Clinical Trials/NCT04058951
NCT04058951UnknownNot Applicable

Dietary Protein Quality and Quantity: Effects of a High Protein Plant-based Diet on Proteinuria Among Patients With Nephropathy - A Randomized Cross-over Trial

Jens Rikardt Andersen2 sites in 1 country20 target enrollmentStarted: August 15, 2019Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Sponsor
Enrollment
20
Locations
2
Primary Endpoint
Urine albumin creatinine ratio (UACR)

Study Overview

Brief Summary

The purpose of this study is to investigate if a diet high in plant protein improves kidney function in patients with kidney insufficiency and diabetes and/or hypertension and/or glomerulonephritis. The study is a non-blinded, randomized, controlled, cross-over-design with two intervention periods of each 14 days. Between the two interventions periods there is a washout period of 14 days. The participants are randomized to start with an individualized diet plan containing either high amounts of animal protein or high amounts of plant protein.

Detailed Description

The purpose of this study is to investigate if a diet high in protein (2,0 g/kg/d) of plant origin, decreases proteinuria amongst patients with diabetes, hypertension and/or glomerulonephritis with presence of micro- or mild macro albuminuria, compared to a diet high in protein of animal origin.

Kidney insufficiency is associated with increased morbidity and mortality, decreased quality of life and large financial costs for the health care system.

Evidence suggest that the source of protein may inflect the progression of the kidney disease where soy protein has shown a positive effect on estimated glomerular filtration rate and proteinuria amongst both diabetic and non-diabetic patients with nephropathy.

The study design is a 6-week, non-blinded cluster randomized, controlled, cross-over study with two intervention periods of each 14 days. Between interventions there is a washout period of 14 days. The participants are randomized to follow either a diet high in plant protein (HPPD) or a diet high in animal protein (HAPD). The diet plans are individualized to accommodate the participants energy requirements. Given the high amount of protein in the diets they are supplemented with either soy protein powder or beef protein powder. To measure primary and secondary endpoint, the participants are instructed to collect two times 24-hour urine sample at the first baseline, after 14 days and after 42 days. Blood samples are collected at the first baseline, after 14 days, at the second baseline and after 42 days.

To gain enough statistical power a minimum of 16 participants should be included. To accommodate a drop-out rate of 25%, 20 participants should be enrolled.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Crossover
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
30 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • UACR between 30 and 800 mg/g in minimum two spot urine samples.
  • Estimated Glomerular Filtration Rate (eGFR) >30 ml/min. eGFR must have been stabil over the past 6 months defined by a maximal fluctuation in eGFR of 10 ml/min.
  • Minimum 30 years of age.
  • Danish speaking and writing
  • No changes in blood pressure medication for the past three months.

Exclusion Criteria

  • Vegetarianism or veganism
  • Pregnancy

Arms & Interventions

High Animal Protein Diet (HAPD)

Placebo Comparator

Consuming a diet high in protein primarily from animal origin.

Intervention: High Animal Protein Diet (HAPD) (Other)

High Plant Protein Diet (HPPD)

Experimental

Consuming a diet high in protein exclusive from plant origin.

Intervention: High Plant Protein Diet (HPPD) (Other)

Outcomes

Primary Outcomes

Urine albumin creatinine ratio (UACR)

Time Frame: 14 days

The change in UACR (assessed by 2 days 24-hour urinal collection) between the two treatment arms

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
Jens Rikardt Andersen
Sponsor Class
Other
Responsible Party
Sponsor Investigator
Principal Investigator

Jens Rikardt Andersen

Associate Professor

University of Copenhagen

Study Sites (2)

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