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Recruiting NCT07544524

Feasibility, Safety and Efficacy of a Predominantly Plant-based Diet in an Asian Population With Chronic Kidney Disease

No phase Interventional Chronic Kidney Disease stage3 Chronic Kidney Disease stage4 Diet Habit

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Predominantly Plant-Based CKD Diet, Standard CKD Diet.
Who it may be relevant to
Registry conditions: Chronic Kidney Disease stage3, Chronic Kidney Disease stage4, Diet Habit. Basic parameters: 21 years — 79 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Singapore
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

This two-year follow up, single-center, open-label, feasibility study will recruit outpatients from the Renal Medicine Clinic at Changi General Hospital. Eligible patients with Stage 3 or 4 CKD will be assigned preferencebased to either a plant-based diet intervention (intake of at least 50% protein from plant sources) with regular dietitian counselling and follow up, or a control group receiving dietitian counselling for general CKD dietary advice without information on percentage of plant-based foods. Six monthly assessments will include estimated glomerular filtration rate (eGFR), serum potassium, nutritional markers, and other relevant biochemical parameters. Quality of life and dietary adherence will be evaluated through questionnaires and food frequency records. This study will evaluate primarily, the feasibility of a plant-based diet in the Singaporean context. Secondarily it will evaluate its safety in terms of incidence of hyperkalaemia, and benefit in terms of improvement in acidosis. Other exploratory outcomes will include (1) preliminary efficacy of plant-based diets on CKD progression (measured by eGFR decline); (2) risk of nutritional deficiencies such as vitamin D, B12 and iron; and (3) impact on other biochemical parameters of CKD.

Interventions

  • Other Predominantly Plant-Based CKD Diet
    Subjects in the intervention group will receive personalised dietary advice \& educational materials from a renal dietitian for retarding CKD progression (low salt, moderate protein) with additional focus on including more non-/minimally processed plant-based foods. Food recommended would be those easily obtained
  • Other Standard CKD Diet
    Subjects in the control arm will receive advice from a renal dietician for general healthy eating for retarding CKD progression (low salt, low-moderate protein intake). No specific advice on percentage of protein intake contributed to by plant-based protein will be given.

Primary outcome measures

  • Adherence to diet - based on Good vs Moderate vs Poor Adherence [Time frame: 1 year]
  • Acceptability of Diet [Time frame: 1 year]
Secondary outcome measures (2)
  • Serum Potassium level in mmol/L [Time frame: 1 year]
  • Serum Bicarbonate Level (mmol/L) [Time frame: 1 year]

Eligibility criteria

Inclusion criteria

  • Age 21-79 (Only adults who can give consent will be recruited. Older adults aged 80 are not included to reduce the risk of confounding due to age-related frailty, sarcopenia and multimorbidity. Additionally, older adults may have different nutritional needs and energy requirements)
  • CKD stage 3-4 (baseline eGFR 15-60ml/min/1.72m2 for the past 6 months)
  • Willingness to see a dietitian and follow either a standard CKD diet or a predominantly plant-based CKD diet
  • On maximum tolerated dose of ACE-inhibitors (Angiotensin converting enzyme inhibitors) or ARB (Aldosterone receptor blocker) as determined by Renal Physician in charge
  • Able to provide informed consent

Exclusion criteria

  • Transplant patients (who will tend to have more variable trajectories, immunosuppression related challenges etc which may make this study less feasible)
  • Pregnant or lactating patients (who have different nutritional requirements than the standard CKD patients)
  • Patients who were on any special diet for at least 1 month prior to recruitment (inclusive of
  • long-term vegans or vegetarians) - excluded because they already have stable dietary habits
  • Age <21 or >/= 80 (Avoid growing children who have different nutritional requirements and advanced elderly who are more likely to have malnutrition or sarcopenia due to other pre-existing causes)
  • Those who have seen a dietitian for CKD previously
  • Patients with severe ischemic heart disease, decompensated liver cirrhosis, malabsorptive diseases or malignancy
  • Patients with BMI <18.5 or >40
  • Patients with glomerulonephritis, genetic kidney disease or polycystic kidney disease
  • Baseline serum potassium 5.0 and above
  • Patients who are unable to modify their diet due to socio-economic issues.
  • Exclude patients with acute kidney injury (AKI) in the past 6 months prior to study (unstable renal disease

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Non-randomized
Model
Parallel assignment
Masking
Open label
Primary purpose
Treatment

Study locations

Singapore · 1 center
  • Changi General Hospital — Singapore

Identifiers

NCT: NCT07544524 · 2025-1195

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗