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Clinical Trials in the USA / NCT07766720
Recruiting Not applicable

Effects of Eggshell Membrane and Curcumin Extract Supplementation, Separately or Combined, on Recovery From Intense Exercise

NCT07766720 · tracked via the Priya Life Science USA tracker
Sponsor
ESM Technologies, LLC
Phase
Not applicable
Started
2026-02-01
Last updated
2026-08-14

Condition(s) studied

Exercise-induced Muscle SorenessExercise-induced Joint PainExercise-induced Joint StiffnessExercise-induced Cartilage Turnover

Investigational drug(s) / intervention(s)

NEM® brand eggshell membrane powdercurQ+® brand highly absorbable curcuminEM PlaceboCurc PlaceboNEM® plus curQ+® combination

NEM® brand eggshell membrane powder: 500 mg/day of NEM® brand eggshell membrane powder in a single #0 capsule.

curQ+® brand highly absorbable curcumin: 2,860 mg/day of curQ+® brand highly absorbable curcumin in a single 10 Oval softgel.

EM Placebo: 500 mg/day of psyllium husk fiber powder in a single #0 capsule.

Curc Placebo: 2,860 mg/day of coconut oil/polysorbate blend in a single 10 Oval softgel.

NEM® plus curQ+® combination: 500 mg/day of NEM® brand eggshell membrane powder in a single #0 capsule PLUS 2,860 mg/day of curQ+® brand highly absorbable curcumin in a single 10 Oval softgel.

Study summary

Eggshell membrane and Curcumin supplementation prior to intense exercise may reduce inflammation, muscle and joint pain, and promote recovery. This proof-of-concept study will examine how ingestion of specially formulated versions of these nutrients affects recovery from intense exercise.

Eligibility

Sex
MALE
Min age
18 Years
Max age
40 Years
Healthy volunteers
Accepted
Inclusion Criteria: * Age 18 to 40 at the time of consent. * Healthy and recreationally active. * Ability to comply with study procedures. * Agree to refrain from alcohol intake and use of non-steroidal anti-inflammatory (NSAIDS), aspirin, and other over-the-counter pain medications for 48 hours prior to and after completion of each testing session. Exclusion Criteria: * No recent history of exercise training * An orthopedic limitation that would prevent the ability to perform the exercise intervention. * Participants who currently smoke cigarettes. * Known allergies to eggs, sulfur, or curcumin.

Primary outcome measure(s)

  • VAS Muscle Soreness Rating — 2 weeks
    Changes in Visual Analog Scale (VAS) ratings of muscle soreness (rated from zero to 100 mm) from baseline following intense exercise. The higher the rating, the more muscle soreness so negative changes in VAS would equate to improvement.

Trial sites (1)

FacilityCityRegionStatus
Exercise & Sport Nutrition Lab - Texas A&M University College Station Texas Recruiting

More ESM Technologies, LLC trials in the USA

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07766720 on ClinicalTrials.gov ↗ ← All trials in the USA