Actively Recruiting
Effect of Menstrual Cycle Phases on Postprandial Triglyceride Concentrations in Healthy Premenopausal Females: A Crossover Study
Led by University of Ottawa · Updated on 2026-05-19
12
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
Sponsors
U
University of Ottawa
Lead Sponsor
N
Natural Sciences and Engineering Research Council, Canada
Collaborating Sponsor
AI-Summary
What this Trial Is About
Researchers are investigating how phases of the menstrual cycle affect post-meal triglyceride levels in healthy young women. The study aims to find out if triglyceride concentrations differ between the early follicular phase and the mid-luteal phase of the menstrual cycle. Participants will attend two experimental sessions where they will consume a high-fat meal representing 33% of their estimated daily energy needs, with 59% of calories from fat. After the meal, they will rest seated for six hours during each session, one in the early follicular phase and one in the mid-luteal phase. Participants will first undergo a screening session to confirm eligibility. During the study sessions, researchers will measure changes in various blood markers including total, buoyant, and denser triglycerides, non-esterified fatty acids, insulin, glucose, and beta-hydroxybutyrate over six hours. Additional outcomes such as hormone levels, energy expenditure, hunger, fullness, and oxidation rates will also be assessed. The study is designed to monitor these effects without randomization or blinding, with total participation spanning the screening and two experimental visits.
CONDITIONS
Brief Title
Postprandial Triglyceride Concentrations Across Menstrual Cycle Phases
Who Can Participate
Eligibility Criteria
You may qualify if you...
- English or French speaking
- Ability to provide informed consent
- Female aged 18 to 30 years
- Healthy premenopausal female with regular menstrual cycles
You will not qualify if you...
- History or evidence of chronic disease
- Current use of hypolipemic medication
- Current use of hormonal contraceptives
- Current use of antidepressants
- Current use of anticoagulants
- Ongoing smoking status
- Experiencing pregnancy, puerperium, or irregular menstrual cycles
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - 1 day
Participants undergo 6 hours of seated rest after consuming a high-fat meal representing 33% of estimated daily energy expenditure during the early follicular phase of their menstrual cycle.
1 visit (in-person)
Duration - 1 day
Participants undergo 6 hours of seated rest after consuming a high-fat meal representing 33% of estimated daily energy expenditure during the mid-luteal phase of their menstrual cycle.
1 visit (in-person)
Trial Site Locations
Total: 1 location
1
Behavioural and Metabolic Research Unit, School of Human Kinetics, Faculty of Health Sciences, University of Ottawa
Ottawa, Ontario, Canada, K1S 5S9
Actively Recruiting
Research Team
P
Pascal Imbeault, PhD
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NON_RANDOMIZED
Model
CROSSOVER
Primary Purpose
BASIC_SCIENCE
Number of Arms
2
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