Progesterone and Muscle Protein Synthesis in Premenopausal Women (MP4-MPS) (MP4 MPS)

McMaster University

Status and phase: Not yet enrolling; Phase 1

Conditions: Healthy Volunteers; Progesterone; Female; Premenopausal

Treatments: Drug: placebo capsule; Drug: Micronized progesterone (oral capsules)

Study type: Interventional

Funder types: Other

Identifiers

NCT07173361

MP4-MPS

Details and patient eligibility

About

The goal of this clinical trial is to learn if micronized progesterone (PROMETRIUM®) influences the muscle-building response to resistance exercise in healthy premenopausal women aged 18-30 years.

The main questions it aims to answer are:

1. Does progesterone change the rate of muscle protein synthesis after exercise?
2. Does progesterone alter the difference in synthesis between an exercised leg and a rested leg?

Researchers will compare micronized progesterone to a placebo to see if progesterone changes the way skeletal muscle adapts to resistance exercise.

Participants will:

• Take two oral doses of progesterone (400 mg total, 34 and 10 hours before testing) or placebo
• Complete a unilateral leg extension exercise session in the lab
• Receive an infusion of a stable isotope tracer and provide blood samples
• Undergo muscle biopsies from the exercised and rested legs

Full description

This is a single-site, randomized, double-blind, placebo-controlled Phase 1 clinical trial designed to evaluate the effects of micronized progesterone on exercise-induced skeletal muscle protein synthesis (MPS) in premenopausal women.

Participants will be healthy, naturally menstruating women aged 18-30 years. Each will be randomized to receive either two oral doses of micronized progesterone (400 mg total, administered as 2 × 200 mg capsules, 34 and 10 hours prior to testing) or a matched placebo.

During the infusion trial, participants will consume a standardized nutritional drink (~530 kcal; 22 g protein, 52 g carbohydrate, 26 g fat) and perform unilateral resistance exercise consisting of single-leg extensions (1 warm-up set followed by 4 working sets to volitional failure, 2-minute rest between sets).

To assess myofibrillar MPS, participants will undergo a primed continuous infusion of L-[ring-¹³C₆]-phenylalanine, with incorporation into muscle proteins determined from serial biopsies collected from both the exercised and rested legs. Blood samples will be obtained throughout the infusion period to measure plasma amino acids and hormone concentrations.

The primary endpoint is the treatment (placebo vs. progesterone) × leg (exercised vs. rested) interaction in MPS over the 5-hour post-exercise period. Secondary outcomes include the exercise-induced change in fractional synthetic rate (ΔFSR), plasma hormone responses, and exploratory measures of body composition and strength.

This study will provide direct evidence on whether progesterone modifies the acute anabolic response to resistance exercise in reproductive-age women, addressing an important gap in female skeletal muscle physiology.

Enrollment: 20 estimated patients

Sex: Female

Ages: 18 to 30 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

1. Self-identifies as female and is assigned female at birth.
2. Aged 18 to 30 years (inclusive).
3. Body mass index (BMI) between 18 and 34.9 kg/m² (inclusive).
4. In general, good health, as determined by a study-specific health screening questionnaire and medical history review.
5. Reports regular menstrual cycles (21-35 days in length) for the past 3 consecutive months.
6. Not currently using hormonal contraceptives and has completed a minimum 3-month washout period.
7. Resting blood pressure <140/90 mmHg at screening and on the infusion day.
8. Willing and able to provide written informed consent in English.

Exclusion criteria

1. Current use of tobacco, vaping products, or nicotine-containing substances.

2. Ineligible for physical activity as determined by the Get Active Questionnaire (GAQ).

3. Any medical, orthopedic, or psychiatric condition that, in the opinion of the Investigator, could interfere with the participant's ability to comply with study procedures or pose additional risk.

4. Current gastrointestinal or swallowing disorders that may interfere with supplement ingestion (e.g., chronic diarrhea, regurgitation, dysphagia).

5. Currently pregnant, planning to become pregnant, or known/suspected to be pregnant.

6. Use of hormonal contraceptives within the past 3 months.

7. Presence of any electronic medical devices or metallic implants that may interfere with DXA scanning or muscle biopsy procedures.

8. History of neuromuscular disorders or muscle/bone wasting diseases.

9. Current or recent use (within 3 months) of medications known to affect protein metabolism (e.g., glucocorticoids, systemic NSAIDs, isotretinoin, or anabolic agents).

10. Personal or first-degree family history of thrombotic events (e.g., DVT, PE, stroke, myocardial infarction).

11. Use of anticoagulant or antiplatelet medications.

12. Excessive alcohol intake (>21 units per week; 1 unit = 10 mL of pure ethanol).

13. History of bleeding disorders or known coagulation or platelet abnormalities.

14. Known hypersensitivity or allergy to micronized progesterone, soya, peanuts, or any excipients in the study capsule.

15. History or current diagnosis of liver dysfunction or hepatic disease, unless liver function tests have returned to normal ranges.

16. History or presence of contraindications to progesterone therapy, including any of the following:

    1. Known or suspected estrogen- or progestin-dependent malignancies (e.g., breast or endometrial cancer).
    2. History of endometrial hyperplasia or unexplained abnormal uterine bleeding.
    3. Active or prior history of arterial thromboembolic disease (e.g., stroke, myocardial infarction, coronary artery disease).
    4. History of classical migraine with aura.
    5. Active or prior history of venous thromboembolism (e.g., deep vein thrombosis, pulmonary embolism) or thrombophlebitis.
    6. History of partial or complete vision loss due to ophthalmic vascular events.

17. Clinically significant anemia or hematologic abnormalities (e.g., low hemoglobin or hematocrit) that may elevate the risk of biopsy complications.

18. Participation in another interventional study involving investigational drugs or invasive procedures within the past 30 days.

19. Documented history of severe vasovagal syncope or needle phobia that may interfere with study compliance or safety.

20. Known allergy or intolerance to any ingredient in the BOOST® 2.24 nutritional drink (e.g., milk protein, soy, corn-derived ingredients, cocoa, or artificial flavorings).

Trial design

Primary purpose: Basic Science

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Quadruple Blind

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20 participants in 2 patient groups, including a placebo group

Experimental: Micronized Progesterone

Experimental group

Description:

Drug - Micronized progesterone (oral capsules; 400 mg total as 2 × 200 mg at \~34 h and \~10 h pre-trial)

Treatment:

Drug: Micronized progesterone (oral capsules)

Placebo Comparator: Placebo

Placebo Comparator group

Description:

Drug - Placebo (oral capsules; matched schedule and appearance)

Treatment:

Drug: placebo capsule