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Taking people in CanadaNo phase

Testing kefir, a fermented milk drink, for heart and immune health

Tests kefir against milk in adults with, or at risk of, type 2 diabetes.

Plain-language title generated from the registry record
Registry title: Improving Health Outcomes With Kefir

Key facts

Where
Edmonton, CanadaSee the site

Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 24 and 70 years old?

Source: NCT06695221, who can take part

Where in Canada

  • University of AlbertaEdmonton, CanadaTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
Print a page for my doctor

Trial details

Who runs it
University of Alberta
Trial code
NCT06695221
Record updated
8 May 2026
Original description
The purpose of the study is to ascertain whether traditional kefir not only enhances vascular health but also contributes to improved immune outcomes in both male and female participants at higher risk or living with Type 2 Diabetes (T2D) after 12 weeks of treatment.Read full original descriptionShow less

Improving Health Outcomes With Kefir

The purpose of the study is to ascertain whether traditional kefir not only enhances vascular health but also contributes to improved immune outcomes in both male and female participants at higher risk or living with Type 2 Diabetes (T2D) after 12 weeks of treatment.

Inclusion: females and males (24-70 years old) living in Edmonton (or Edmonton area/driving distance); overweight or obesity (BMI >25 Caucasian, >23 Asian); at higher risk of T2D (fasting blood glucose ≥ 5.6 - 6.9 mmol/L or/and HbA1C ≥ 5.5 - 6.4%); or; with diagnosis of T2D (fasting blood glucose ≥ 7.0 mmol/L or/and HbA1C ≥ 6.5%).

Exclusion: use of medications within the last 3 months (i.e., antibiotics or antifungals, corticosteroids, methotrexate, or immunosuppressive cytotoxic agents); gastrointestinal (GI) disorders of any kind; monogenic dyslipidemias and endocrine disorders except for diabetes; any health conditions deemed to interfere with primary outcomes at the investigator's discretion (e.g., kidney disease, liver disease, cancer, GI surgery, heavy alcohol consumption, etc.); a usual high intake (maximum intake 3 servings/week) of fermented foods excluding cheese (i.e., kefir, kombucha, kimchi, etc.) for the past 3 months; being pregnant or breastfeeding; having a pacemaker or any electrical medical device that prevents the individual from undergoing the bioelectrical impedance analysis bioimmunoassay (BIA) test.".

ClinicalTrials.gov NCT06695221