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Recruiting NCT07544524

NCT07544524 Feasibility, Safety and Efficacy of a Predominantly Plant-based Diet in an Asian Population With Chronic Kidney Disease

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Clinical Trial Summary
NCT ID NCT07544524
Status Recruiting
Phase
Sponsor Changi General Hospital
Condition Chronic Kidney Disease stage3
Study Type INTERVENTIONAL
Enrollment 40 participants
Start Date 2026-04-01
Primary Completion 2027-09-30

Eligibility & Interventions

Sex All sexes
Min Age 21 Years
Max Age 79 Years
Study Type INTERVENTIONAL
Interventions
Predominantly Plant-Based CKD DietStandard CKD Diet

Eligibility Fast-Check

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What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 40 participants in total. It began in 2026-04-01 with a primary completion date of 2027-09-30.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

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.

Eligibility Criteria

Inclusion Criteria: 1. 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) 2. CKD stage 3-4 (baseline eGFR 15-60ml/min/1.72m2 for the past 6 months) 3. Willingness to see a dietitian and follow either a standard CKD diet or a predominantly plant-based CKD diet 4. On maximum tolerated dose of ACE-inhibitors (Angiotensin converting enzyme inhibitors) or ARB (Aldosterone receptor blocker) as determined by Renal Physician in charge 5. 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

Frequently Asked Questions

Who can join the NCT07544524 clinical trial?

This trial is open to participants of all sexes, aged 21 Years or older, up to 79 Years, studying Chronic Kidney Disease stage3. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07544524 currently recruiting?

Yes, NCT07544524 is actively recruiting participants. Visit ClinicalTrials.gov or contact Changi General Hospital to inquire about joining.

Where is the NCT07544524 trial being conducted?

This trial is being conducted at Singapore, Singapore.

Who is sponsoring the NCT07544524 clinical trial?

NCT07544524 is sponsored by Changi General Hospital. The trial plans to enroll 40 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: September 2026  ·  Data Methodology