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RecruitingNCT06155708Updated Jan 22, 2025

Exogenous Ketone Supplementation in Females with Polycystic Ovary Syndrome

An interventional study of Ketone and Water in PCOS, sponsored by McGill University. Recruiting at 1 site in Canada. Open to participants aged 18 Years to 40 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2025-01-22.

Sponsored by McGill University · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
60
Allocation
Randomized
Ages
18 Years to 40 Years
Sex
All
01

Study summary

Polycystic ovary syndrome (PCOS) affects 1 in 5 females of reproductive age. Commonly characterized as a disorder of infertility, PCOS is often accompanied by 3 potent cardiovascular disease (CVD) risk factors: insulin resistance, endothelial dysfunction, and elevated blood pressure. Accordingly, PCOS is associated with the development of CVD, the second leading cause of death in females in Canada. However, effective treatments to improve cardiovascular health in PCOS are lacking.

Exogenous ketone monoester (KME) ingestion has been shown to improves outcomes associated with insulin resistance, endothelial function, and blood pressure regulation in healthy individuals and individuals predisposed to CVD. Therefore, oral ketone supplements offer a practical and effective strategy for improving cardiovascular health; however, this treatment has yet to be evaluated in PCOS.

Therefore, the overall goal of this project is to employ KME ingestion to improve markers of cardiovascular health in females with PCOS.

On two different days, participants will consume either a beverage containing a ketone supplement or a beverage containing a placebo supplement. The objectives are to compare responses between KME and placebo ingestion, and examine all outcomes related to cardiovascular health in females with PCOS in comparison with female controls of similar age and body mass index. The effects of KME ingestion will be quantified on: 1) glycemic control during an oral glucose tolerance test; 2) endothelial function using the flow-mediated dilation test; 3) blood pressure and acute blood pressure regulation; and 4) hemodynamic responses to acute exercise.

02

Conditions studied

  • PCOS

Keywords

  • Polycystic ovary syndrome
  • Ketone monoester ingestion
  • Insulin resistance
  • Endothelial function
  • Blood pressure
  • Oral glucose tolerance test
  • Flow mediated dilation
  • Handgrip exercise
  • Neurovascular transduction
  • Cold pressor test
03

In context

Polycystic Ovary Syndrome

944 studies on the registry are indexed under Polycystic Ovary Syndrome; 174 are open to participants now.

This study's planned enrollment of 60 is below the median of 70 across 685 interventional studies indexed under Polycystic Ovary Syndrome.

Browse Polycystic Ovary Syndrome studies →

Lead sponsor

McGill University is the lead sponsor of 244 studies on the registry; 49 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 40 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • All female participants will report female sex assigned at birth
  • All participants will be aged 18 to 40
  • PCOS diagnosis

Exclusion criteria

Exclusion Criteria:

  • Current smokers or a prolonged history of smoking
  • Presence or history of overt cardiometabolic disease (e.g., stage 2 hypertension, diabetes, heart disease), neurologic disease, or endocrinopathy (with the exception of PCOS)
  • Current pregnancy or currently breastfeeding
  • Current use of medications which may affect our outcomes of interest (e.g., anti-hypertensives, anti-androgens, metformin)
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Crossover assignment
Masking
Double (Participant, Investigator)
Enrollment
60 participants (estimated)

Study arms

  • Experimental
    Ketone

    - Ketone monoester supplement in the form of (R)-3-hydroxybutyl (R)-3-hydroxybutyrate based on participants' body weight (0.45ml/kg body weight) ingested with water and vanilla-flavored stevia in a total volume of 100 ml.

    Dietary Supplement: Ketone

  • Placebo comparator
    Placebo

    100 ml water combined with 10ml bitter flavor and vanilla-flavored stevia

    Dietary Supplement: Water

Interventions

  • Dietary supplementKetone

    - Ketone monoester supplement in the form of (R)-3-hydroxybutyl (R)-3-hydroxybutyrate based on participants' body weight (0.45ml/kg body weight) ingested with water and vanilla-flavored stevia in a total volume of 100 ml.

  • Dietary supplementWater

    100 ml water combined with 10ml bitter flavor and vanilla-flavored stevia

06

What researchers measure

Primary outcomes

  1. Glycemic responses to a 2-hr oral glucose tolerance test

    - Glucose is calculated by the area under the curve using the trapezoid method.

    Time frame: 0-2.5 hours in the post-prandial period

  2. Flow mediated dilation (FMD)

    - Endothelial function is assessed using the standard FMD; quantified as the percent increase in diameter from rest to peak diameter observed during reactive hyperemia (%FMD). The % change in diameter reflects the ability of the vessel to dilate in response to sheer stress induced by the flow following the release of occlusion. This reflects the function of the endothelium, or release of nitric oxide.

    Time frame: 30 minutes

  3. Systolic Blood Pressure (SBP)

    - SBP, measured in mmHg

    Time frame: 2 hours

  4. Diastolic Blood Pressure (DBP)

    - DBP, measured in mmHg

    Time frame: 2 hours

Secondary outcomes

  1. Insulin area under the curve

    - Insulin area under the curve during oral glucose tolerance test

    Time frame: 0-2.5 hours in the post-prandial period

  2. C-peptide

    - C-peptide area under the curve during oral glucose tolerance test

    Time frame: 0-2.5 hours in the post-prandial period

  3. Glucagon-like peptide-1 (GLP-1)

    - GLP-1 area under the curve during oral glucose tolerance test.

    Time frame: 0-2.5 hours in the post-prandial period

  4. Glucose-dependent insulinotropic polypeptide (GIP)

    - GIP area under the curve during oral glucose tolerance test.

    Time frame: 0-2.5 hours in the post-prandial period

  5. Triglycerides

    - Triglycerides area under the curve during oral glucose tolerance test

    Time frame: 0-2.5 hours in the post-prandial period

  6. Insulinogenic index

    - (Insulin at 30 min - fasting insulin)/ (plasma glucose at 30 min- fasting plasma glucose).

    Time frame: 0-2.5 hours in the post-prandial period

  7. Arterial artery blood flow

    - Calculated as the product of mean blood flow velocity (cm/sec) and cross-sectional area (2Πr2) x 60 sec/min.

    Time frame: 0-2.5 hours in the post-prandial period

  8. Shear rate and low-flow mediated vasoconstriction to the FMD

    - Shear rate calculated as area under the curve from cuff deflation to the time of peak dilation using the trapezoidal rule, as well as low flow-mediated vasoconstriction during forearm occlusion, which provides an index of the endothelial contribution to resting vascular tone and which predicts cardiovascular disease risk.

    Time frame: 30 minutes

  9. Muscle sympathetic nerve activity (MSNA)

    - Measured using microneurography, and expressed in burst/min or bursts/100 heart beats

    Time frame: 2 hours

  10. Neurovascular transduction

    - Assessed by the MSNA signal (recorded in both raw and filtered/rectified/integrated formats for subsequent analyses) and arterial blood flow extracted on a beat-by-beat basis and processed using custom transduction software.

    Time frame: 2 hours

  11. Vascular resistance

    - Calculated as mean arterial pressure divided by Finometer-derived cardiac output

    Time frame: 2 hours

  12. Capillary blood Beta-OHB concentrations

    - Measures in mmol/L

    Time frame: 0-2.5 hours in the post-prandial period

  13. Serum testosterone

    - Measured in pg/ml.

    Time frame: 5 minutes

  14. Serum sex hormone binding globulin

    - Measured in pg/ml.

    Time frame: 5 minutes

  15. Serum estradiol

    - Measured in pg/ml.

    Time frame: 5 minutes

  16. Serum Progesterone

    - Measured in pg/ml.

    Time frame: 5 minutes

07

Study locations

1 of 1 sites recruiting
  • Cardiovascular Health and Autonomic Research Laboratory
    Montréal, Quebec H2W 1S4, Canada
    Recruiting
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jan 22, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06155708
Lead sponsor
McGill University
Responsible party
Charlotte Usselman (Primary Investigator, McGill University) — Principal investigator
First posted
Dec 4, 2023
Start date
Jan 20, 2025 (estimated)
Primary completion
Jun 2027 (estimated)
Completion
Dec 2027 (estimated)
Last update
Jan 22, 2025

Study contacts

Charlotte Usselman, Ph.D
Contact
charlotte.usselman@mcgill.ca
5143962140
Charlotte Usselman, Ph.D
principal investigator · McGill University

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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