Time-Restricted eating tested as kidney disease therapy

NCT ID NCT06618859

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Recruiting now This study
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Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
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Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

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Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
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Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

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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

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

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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

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  1. The places running it

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  2. The official record

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Contacts and locations

Locations

  • University Hospital, Geneva

    RECRUITING

    Geneva, 1211, Switzerland

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