Chronic Kidney Disease Trial, Recruiting NCT06618859 Sponsor: de Seigneux Sophie Condition: Chronic Kidney Disease
Back to Chronic Kidney Disease

Chronic Kidney Disease Trial, Recruiting

NCT06618859
Recruiting Not Applicable

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • Adults (men and women)
  • People who have been diagnosed with Chronic Kidney Disease at a moderate stage, specifically with a kidney filtration rate between 30 and 90 mL/min/1.73m² (known as KDIGO stage G2 or G3)
  • People who have a moderate-to-high level of protein (albumin) in their urine, within a specific range of 3 to 200 mg/mmol, but not at the highest ("nephrotic") levels
  • People with a body weight in the range considered moderate, specifically a Body Mass Index (BMI) between 18 and 40
  • People whose current daily eating window spans about 12 hours (meaning all meals and snacks are consumed within a 12-hour period each day, as reported by the person and confirmed during a preparation phase)
  • People who are able to understand and agree to the study procedures and commit to the full duration of the trial
  • People who are comfortable using a smartphone (compatible with iOS or Android) and able to regularly photograph their food and drinks using a specific app called MyFoodRepo

Who may not be able to join:

  • Women who are pregnant, breastfeeding, or planning to become pregnant during the study
  • People who have a diagnosed eating disorder
  • People who are currently following a low-carbohydrate, ketogenic, or calorie-restricted diet (note: exclusions for food intolerances, or vegan or vegetarian diets, do not apply here)
  • People with high blood pressure that is not well controlled (above 160/100 mmHg)
  • People who have diabetes and are taking medications that can cause low blood sugar (hypoglycemia) — however, people with prediabetes, or diabetes managed without such medications or with no medication at all, may still be considered
  • People currently taking oral corticosteroid medications (steroid tablets)
  • People with poorly controlled diabetes, indicated by a blood sugar marker (HbA1c) above 8.5%
  • People with an active cancer diagnosis or who have received cancer treatment within the past 12 months
  • People with a major mental illness
  • Women who drink more than 7 standard alcoholic drinks per week, or men who drink more than 14 standard alcoholic drinks per week
  • People who work evening or night shifts, or who plan to do so during the study
  • People who plan to travel to a time zone that differs by 2 or more hours during the study
  • People whose kidney-related or other relevant medications have been changed in the last 3 months (including, but not limited to, ACE inhibitors, SGLT2 inhibitors, or finerenone)
  • People who have recently been diagnosed with a kidney inflammation condition (glomerulonephritis) and are taking more than 2 immune-suppressing medications
  • People who have received a kidney transplant within the past year
  • People who are currently enrolled in, or have been enrolled in, another clinical trial involving a medication or medical device within the past month, or who plan to join one during the study

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 7 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

Contact this trial

Principal Investigator: Sophie de Seigneux, MD, PhD, University Hospital, Geneva

Phone: +41-22-3723311

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Not Applicable
Sponsor
de Seigneux Sophie
Registry
ClinicalTrials.gov
Start date
4 December 2024
Est. completion
1 March 2027

Where this trial is recruiting

🇨🇭 Switzerland

Primary endpoints

Change in urine albumin/creatinine ratio (UACR)

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 7 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov