ClinicalTrials.gg
RecruitingNCT07766720Updated Aug 14, 2026

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

An interventional study of NEM® brand eggshell membrane powder and curQ+® brand highly absorbable curcumin in Exercise-induced Muscle Soreness, Exercise-induced Joint Pain and Exercise-induced Joint Stiffness, sponsored by ESM Technologies, LLC. Recruiting at 1 site in United States. Open to male participants aged 18 Years to 40 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-08-14.

Sponsored by ESM Technologies, LLC · Not applicable, Interventional, and Prevention

From the registry’s dates

  • Registered 5 months after the study started (first participant enrolled Feb 2026, registered Jul 2026).
  • Started Feb 2026; still recruiting 9 months later.
Phase
Not applicable
Study type
Interventional
Enrollment
60
Allocation
Randomized
Ages
18 Years to 40 Years
Sex
Male
01

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.

Read the detailed description

Eggshell membrane (EM) is derived from the inner fibrous layer of eggs that contain a number of proteins and Types I, V, and X collagen and sulfur containing amino acids (i.e., e.g., methionine, cysteine), glycosaminoglycans (e.g., hyaluronic acid, dermatan sulfate, chondroitin sulfate) that are found in synovium, cartilage, ligaments, and tendons of human joint tissue. Initial studies have shown that EM supplementation reduces inflammation and perception of pain while improving markers of joint health in individuals with osteoarthritis. Curcumin (Curcuma longa) is a member of the ginger family (Zingiberaceae) that contains polyphenols that have anti-inflammatory properties. Studies show that curcumin (Curc) can reduce inflammation related to osteoarthritis, exercise, concussion and traumatic brain injury. Theoretically, EM and Curc supplementation prior to intense exercise may reduce inflammation, perceptions of muscle and joint pain, and promote recovery. This proof-of-concept study will examine how ingestion of specially formulated versions of these nutrients (NEM® brand eggshell membrane and curQ+® brand highly absorbable curcumin) separately and in combination affects recovery from intense exercise in recreationally active men.

02

Conditions studied

  • Exercise-induced Muscle Soreness
  • Exercise-induced Joint Pain
  • Exercise-induced Joint Stiffness
  • Exercise-induced Cartilage Turnover

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Keywords

  • intense exercise
  • NEM
  • curQ+
  • eggshell membrane
  • curcumin
03

In context

Arthralgia

277 studies on the registry are indexed under Arthralgia; 54 are open to participants now.

This study's planned enrollment of 60 is below the median of 73 across 218 interventional studies indexed under Arthralgia.

Browse Arthralgia studies →

Lead sponsor

ESM Technologies, LLC is the lead sponsor of 13 studies on the registry; 3 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
Male
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

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

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.
05

Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Quadruple (Participant, Care provider, Investigator, Outcomes assessor)
Enrollment
60 participants (estimated)

Study arms

  • Experimental
    Active, EM

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

    Dietary Supplement: NEM® brand eggshell membrane powder · Dietary Supplement: Curc Placebo

  • Experimental
    Active, curc

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

    Dietary Supplement: curQ+® brand highly absorbable curcumin · Dietary Supplement: EM Placebo

  • Placebo comparator
    Placebo

    500 mg/day of psyllium husk fiber powder in a single #0 capsule PLUS 2,860 mg/day of coconut oil/polysorbate blend in a single 10 Oval softgel.

    Dietary Supplement: EM Placebo · Dietary Supplement: Curc Placebo

  • Experimental
    Active, EM+Curc

    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.

    Dietary Supplement: NEM® plus curQ+® combination

Interventions

  • Dietary supplementNEM® brand eggshell membrane powder

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

  • Dietary supplementcurQ+® brand highly absorbable curcumin

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

  • Dietary supplementEM Placebo

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

  • Dietary supplementCurc Placebo

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

  • Dietary supplementNEM® 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.

06

What researchers measure

Primary outcomes

  1. VAS Muscle Soreness Rating

    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.

    Time frame: 2 weeks

Secondary outcomes

  1. Urinary CTX-II

    Changes in urinary CTX-II biomarker from baseline following intense exercise.

    Time frame: 2 weeks

  2. Muscle Damage

    Changes in markers of muscle enzyme efflux/damage (CK, LDH) from baseline following intense exercise.

    Time frame: 2 weeks

  3. Exercise Performance

    Changes in exercise performance (strength, muscular endurance, peak aerobic capacity) from baseline following intense exercise.

    Time frame: 2 weeks

  4. Inflammation Biomarkers

    Changes in markers of inflammation (TNFα, interleukin (IL) cytokines (IL-1β, IL-2, IL-4, IL-5, IL-6, IL-8, IL-10) from baseline following intense exercise.

    Time frame: 2 weeks

07

Study locations

1 of 1 sites recruiting
  • Exercise & Sport Nutrition Lab - Texas A&M University
    College Station, Texas 77843, United States
    Recruiting
    • Richard B. Kreider, Ph.D. · Contactrbkreider@tamu.edu · (979) 458-1498
    • Christopher Rasmussen, M.S. · Contactcrasmussen@tamu.edu · (979) 458-1498
    • Richard B. Kreider, Ph.D. · Principal investigator
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 Aug 14, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07766720
Lead sponsor
ESM Technologies, LLC
Collaborators
Exercise & Sport Nutrition Lab, Texas A&M University
Responsible party
Sponsor
First posted
Aug 14, 2026
Start date
Feb 1, 2026
Primary completion
Oct 15, 2026 (estimated)
Completion
Dec 31, 2026 (estimated)
Last update
Aug 14, 2026

Study contacts

Richard B. Kreider, Ph.D.
Contact
rbkreider@tamu.edu
(979) 458-1498
Christopher Rasmussen, M.S.
Contact
crasmussen@tamu.edu
(979) 458-1498
Richard B. Kreider, Ph.D.
principal investigator · Exercise & Sport Nutrition Lab, Texas A&M University
Kevin J. Ruff, Ph.D.
study director · ESM Technologies, LLC

Oversight

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

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