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NCT05968391Active, not recruiting

Acetoacetate and Acetate Metabolism in Patients With Chronic Kidney Failure.(RENO-TEP)

Comparison of Acetoacetate and Acetate Kidney Uptake in Patients With Chronic Kidney Failure Measured by Positron Emission Tomography : the RENO-TEP Project

Source: ClinicalTrials.gov · Last updated 22 Oct 2026

Brief summary (registry, in English)

The objective of this study is to nake a comparison between 11c-acetate and 11c-acetoacetate kidney uptake in chronic kidney failure patients.

Status (registry)
Active, not recruiting
Study type
Observational
Enrollment
15 (estimated)
First submitted
20 Jul 2023
Start date
2 Feb 2024
Primary completion date
15 Dec 2026
Lead sponsor
Université de Sherbrooke
NCT number
NCT05968391

What you commit to

  • Study type: Observational
  • Planned participants: 15
  • From 2 Feb 2024 to the primary completion date, 15 Dec 2026
  • 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

  • Receive cytotoxic therapy for primary or secondary kidney disease within 6 months prior to enrollment
  • Organ Transplant History
  • Myocardial infarction, unstable angina, stroke or transient ischemic attack within 12 weeks prior to enrollment

Other illness

  • Class IV congestive heart failure (New York Heart Association)
  • Any condition outside the realm of renal and cardiovascular disease, such as, but not limited to, malignancy, with a life expectancy of less than 2 years in the clinical judgment of the investigator
  • Active malignancy requiring treatment at Visit 1 (except successfully treated basal or squamous cell carcinoma).

Lab values

  • Hepatic impairment (aspartate transaminase or alanine transaminase \>3x upper limit of normal; or total bilirubin \>2x upper limit of normal at time of enrollment

Other

  • Coronary revascularization (percutaneous coronary intervention or arterial bypass) or valve repair/replacement within 12 weeks of enrollment or is scheduled to undergo one of these procedures within 4 weeks of enrollment
  • Pregnancy or lactation
  • Adherence to a ketogenic diet, consumption of ketogenic products or supplements or intermittent fasting or other diet or supplements that may significantly increase ketones in the past two months.
  • Daily alcohol consumption \>2 servings per day
  • Participation in other interventional research projects concurrently or participation in other PET research projects in the last year, which exceeds the recommended limits
  • Inability to lie still in supine position;
  • Medical fluid restriction limiting fluid intake for the procedure

Who the study is looking for

  • BMI between 18.5 and 40
  • Kidney failure if GFR betweem 30 and 60 mL/min/1.73m2
  • Stable medication for at least 4 weeks

Age in the registry: 18 years to - · 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
Centre de recherche sur le vieillissement
Coordinator of this site? Confirm its status
SherbrookeCanadaUnknown status

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