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NCT06884059RecruitingPhase 1

Time Restricted Eating in Patients With Microalbuminuria

Impact of Time-Restricted Eating (TRE) on Kidney Health (The TREK Study)

Source: ClinicalTrials.gov · Last updated 14 Jul 2026

Brief summary (registry, in English)

This is a clinical trial to assess how time-restricted eating (TRE) may improve kidney health and filtration patients with type 2 diabetes and increased protein content in their urine. All participants will be participating in TRE in which they follow a consistent 8-10 hour eating window everyday.

Status (registry)
Recruiting
Phase (registry)
Phase 1
Study type
Interventional
Enrollment
25 (estimated)
First submitted
5 Mar 2025
Start date
Jul 2026
Primary completion date
Feb 2027
Lead sponsor
University of California, San Diego
NCT number
NCT06884059

What you commit to

  • Study type: Interventional · Phase 1
  • Planned participants: 25
  • From Jul 2026 to the primary completion date, Feb 2027
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Systolic BP greater than 160 mmHg and/or Diastolic BP greater than 110 mmHg (with or without treatment/medication)
  • Active tobacco or illicit drug use
  • Currently on a special or prescribed diet for other reasons (e.g., Celiac disease),
  • On recently prescribed medication that is meant for weight loss, or has known effect on appetite suppression ( patient on stable dose for 3 months can be enrolled ).

Other illness

  • History of eating disorder(s).
  • History of surgical intervention for weight management (e) active eating disorder.
  • Treatment for active inflammatory and/or rheumatologic disease and cancer.
  • A major adverse cardiovascular event within the past 6 months such as acute coronary syndrome (ACS), percutaneous coronary intervention, coronary artery bypass graft surgery, hospitalization for congestive heart failure, stroke/transient ischemic attack (TIA).
  • History of Uncontrolled arrhythmia (i.e., rate-controlled atrial fibrillation/atrial flutter are not exclusion criteria) 18. Liver cirrhosis and/or significant alterations in liver function
  • History of (a) thyroid disease requiring dose titration of thyroid replacement medication(s) within the past 3 months (i.e., hypothyroidism on a stable dose of thyroid replacement therapy is not an exclusion), Shift workers with variable (e.g., nocturnal) hours.
  • History of major adverse cardiovascular events within the past 1 year (acute coronary syndrome (ACS), percutaneous coronary intervention, coronary artery bypass graft surgery, hospitalization for congestive heart failure, stroke/transient ischemic attack (TIA)).
  • History of thyroid disease requiring dose titration of thyroid replacement medication(s) within the past 3 months (i.e., hypothyroidism on a stable dose of thyroid replacement therapy is not an exclusion).
  • History of adrenal disease.
  • History of malignancy undergoing active treatment, except non-melanoma skin cancer.
  • Known history of type I diabetes.
  • History of stage 4 or 5 chronic kidney disease or requiring dialysis.
  • History of HIV/AIDS.
  • Uncontrolled psychiatric disorder (including history of hospitalization for psychiatric illness).

Lab values

  • Participants with Type1DM and T2DM who are taking insulin, sulfonylureas, or have an HbA1c \> 9 %.
  • Estimated Glomerular Filtration Rate (EGFR) \< 45
  • LDL cholesterol greater than 200 mg/dL
  • Triglycerides greater than 500 mg/dL
  • Chronic kidney disease with an eGFR calculated based on the Modification of Diet in Renal Disease (MDRD) equation \<50mL/min/1.73m2

Other

  • Pregnant or breastfeeding individuals.
  • Currently enrolled in a weight-loss or weight-management program,
  • Caregivers for dependents requiring frequent nocturnal care/sleep interruptions.
  • More than one trip planned to travel to a time zone with greater than a 3-hour difference during study period.

Who the study is looking for

  • Age: 18-75 years old
  • Participants with T2DM with A1c between 6.5 and 9.0 % and on stable doses of medications who are weight-bearing and self-ambulatory.
  • uACR ( urine albumin creatinine ratio) results ≥ 30 - 300 mg.
  • Willingness to use smartphone for research procedures (Apple iOS or Android OS)
  • Baseline eating period ≥12 hours/day and sufficient logging on the mCC app.
  • Person of childbearing potential will be given a pregnancy test on study enrollment and asked to use contraception throughout the study.
  • Post-menopausal and individuals on hormone replacement therapy will be included.
  • Estimated Glomerular Filtration Rate (EGFR) \> 45
  • If participants are on cardiovascular medications (HMG CoA reductase inhibitors (statins), other lipid-modifying drugs, anti-hypertensives) no dose adjustments will be allowed during the study period
  • Participants on stable doses (consistent dose for ≥3 months) of GLP-1 receptor agonists will be included.

Age in the registry: 18 years to 75 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Altman Clinical and Translational Research Institute
Coordinator of this site? Confirm its status
La JollaUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.