Time-Restricted eating tested as kidney disease therapy
NCT ID NCT06618859
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This pilot study tests whether time-restricted eating (eating all meals within an 8-hour window each day) can reduce protein in the urine and slow kidney function decline in people with moderate chronic kidney disease. Fifty adults with stage 2-3 CKD and elevated albuminuria will follow either the 8-hour eating plan or their usual eating pattern for 12 weeks. Researchers will measure changes in kidney markers, blood pressure, body composition, and safety.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- time-restricted eating (behavioral intervention)
- What this could lead to
- If successful, this could point toward a simple dietary strategy to help manage chronic kidney disease and reduce protein leakage.
- What could go wrong
- This is a small pilot study with only 50 participants, so results may not apply broadly. Dietary changes can be hard to maintain, and the effect on kidney function may be modest or absent.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
-
About 50 people
The number the study aims to enrol. It can still change while the study runs.
- Started
-
Dec 2024
- Expected to finish
-
Dec 2027
An estimate. End dates often move.
- Lead sponsor
-
Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
18 years and older
- Sex
-
Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Clinical criteria * Adult men and women * Chronic Kidney Disease with KDIGO stage G2 and G3 defined by a Glomerular Filtration Rate between 30 and 90 mL/min/1.73m2 * Albuminuria stage A2 or A3, but without nephrotic-range proteinuria: 3 to 200 mg/mmol * Body mass index 18-40 kg/m2 * Eating window of 12 hours (self-reported and measured during the run-in phase) * Study-related criteria * Able to give informed consent and follow the study procedures for the entire duration * Confident use of a smartphone compatible with the MyFoodRepo app (iOS, Android) and able to take regular pictures of food/drinks Exclusion Criteria: * Clinical criteria * Pregnant and breastfeeding women, plans for maternity during the study * Eating disorder(s) * Other diets: low-carb, ketogenic diet, hypocaloric diets (eviction for food intolerances, vegan/vegetarian diet are not excluded) * Uncontrolled blood pressure (\> 160/100 mmHg) * Diabetes with hypoglycemic drug(s) will be excluded, however those with impaired glucose tolerance (prediabetes, as defined by the American Diabetes Association) or diabetes with no risk of hypoglycemia (i.e. treated with non-hypoglycemic drugs or without medication) will be included * Oral corticosteroids * Uncontrolled diabetes HbA1c \> 8.5% * Active cancer and/or oncologic treatment over the previous 12 months * Major mental illness * Consumption of \> 7 standard units of alcohol per week for women and \> 14 standard units of alcohol per week for men * Shift work, such as evening shifts or night shifts planned during the study * Travel/trip to a different time zone (≥ 2-hour time difference) planned during the study * Study-related criteria and other interventions * Recent treatment modification in the last 3 months, including but not limited to ACE blockers, SLGT2i, finerenone * Patients with recent glomerulonephritis diagnosis on more than 2 immunosuppressive drugs * Patients with kidney transplant in the last past year * Enrolled in another interventional clinical trial (medication, medical device) over the previous 1 month and planned during the study
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for Renal insufficiency chronic are added.
By submitting, you agree to our Terms of use
Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
-
The places running it
1 site. The list below names each one and where it is.
-
The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
-
A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
-
University Hospital, Geneva
RECRUITINGGeneva, 1211, Switzerland
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Can calming inflammation shield the heart?
- Can a kidney drug stop acute injury from becoming chronic?
- Could your bone health decide if a dental implant lasts?
- Can a pharmacist check-in boost medication adherence in diabetes and kidney disease?
- Kidney disease in young women: a hidden burden on fertility and future plans
- New drug combo aims to slow kidney failure in High-Risk patients