Actively Recruiting

Phase Not Applicable
Age: 18Years - 30Years
FEMALE
Healthy Volunteers
ID07459465

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

Age: 18Years - 30Years
FEMALE
Healthy Volunteers

Eligibility Criteria

Eligible

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
Not Eligible

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

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Early Follicular Phase

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)

Mid-Luteal Phase

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

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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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