Clinical trial Recruiting at 1 site Interventional Ages 18 and up

Whole milk versus skim milk effects on cholesterol and blood sugar

Official title: Gauging Outcomes of Total Milk Ingestion on Lipid and gControl

Run by University of California, San Francisco · NCT07087184 · Data updated 2026-11-12

This trial will test whether drinking whole milk or skim milk for two months at a time changes cholesterol and insulin resistance in adults who regularly drink milk.

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Quick facts

Study typeInterventional
Ages18 Years and up
SexAll
Enrollment110 (estimated)
SponsorUniversity of California, San Francisco
Academic / other
Locations1 site (San Francisco, California)
StatusRecruiting
StartedJuly 24, 2025
Main results expectedJune 2027
Study endsAugust 2027
Registry record updatedOctober 2, 2026
Trial IDNCT07087184 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are adults (≥18) who regularly drink at least one cup of dairy milk most days, have a smartphone, can use the Eureka app, are English-speaking, and do not have diabetes, lactose intolerance, recent myocardial infarction, or familial hypercholesterolemia.

Probably not a fit

People with type 1 or type 2 diabetes, lactose intolerance, familial hypercholesterolemia, a history of myocardial infarction, or those planning to change cholesterol treatment are excluded and unlikely to benefit from this protocol.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This is an N-of-1 randomized crossover trial in which each participant is assigned to limit their liquid milk to whole milk for two months and then skim milk for two months, or the reverse order. Lab tests including hemoglobin A1c and fasting lipids are performed at two and four months to measure changes in glycemic markers and blood lipids. Participants use the Eureka mobile app and continuously wear a wrist fitness tracker, Bluetooth scale, and blood pressure monitor to record weight, blood pressure, activity, and milk intake while keeping other aspects of their diet constant. A total of 100 adults who regularly consume at least one cup of milk daily will be enrolled at UCSF.

Why it matters

Potential benefit: If successful, the results could help milk-drinking adults and their clinicians choose whole versus skim milk to better manage cholesterol and markers of insulin resistance.

How similar studies have gone: Prior observational and randomized work on dairy fat and cardiometabolic risk has been mixed, and N-of-1 randomized crossover trials comparing whole versus skim milk are relatively novel.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Are age ≥18 years
* Have a smartphone
* Are able to use the Eureka mobile application
* Consume, on average, at least one cup of dairy milk daily, at least 5 days per week

Exclusion Criteria:

* Non-English speaker
* Are lactose intolerant
* History of myocardial infarction
* History of type I or type II diabetes
* Familial hypercholesterolemia
* Plan to change treatment for cholesterol
* Are pregnant or plan on getting pregnant
* Unable to read or sign to provide informed consent

Where it's running

  • UCSF Medical Center at Parnassus
    San Francisco, California, United States
    Recruiting

Study contacts

  • Principal investigator: Gregory M Marcus, MD, MAS — University of California, San Francisco
  • Study coordinator: Gregory M Marcus, MD, MAS
  • Email: greg.marcus@ucsf.edu
  • Phone: 415-476-5706

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.