Status:

COMPLETED

A Randomized, Double-Blind, Controlled Trial to Assess the Efficacy of a Fortetropin Supplement in Improving Symptoms of Osteoarthritis

Lead Sponsor:

MYOS Corp

Collaborating Sponsors:

Citruslabs

Conditions:

Osteoarthritis

Eligibility:

All Genders

50-75 years

Phase:

NA

Brief Summary

This is a hybrid, double-blind, randomized, placebo-controlled clinical trial that will last 12 weeks. Participants will be randomized into either the intervention product or control group and will co...

Eligibility Criteria

Inclusion

  • Men and women aged 50-75 years of age
  • Self-reporting osteoarthritis-like symptoms, experiencing 3 or more of the following symptoms: joint pain, inflammation, reduced mobility, joint swelling, and stiffness.
  • Non-acute osteoarthritis, must have experienced symptoms for longer than 1 year.
  • Generally healthy and don't live with any uncontrolled chronic disease
  • Able to eat eggs (haven't been medically advised to avoid)
  • Willing to stop eating eggs for the 12 week study

Exclusion

  • Anyone allergic or intolerant of eggs
  • Anyone who has been advised to avoid eggs
  • Any pre-existing chronic conditions that would prevent participants from adhering to the protocol, including oncological and psychiatric disorders.
  • Anyone with known severe allergic reactions.
  • Women who are pregnant, breastfeeding or attempting to become pregnant
  • Unwilling to follow the study protocol.
  • Subjects currently enrolled in another clinical study
  • Subjects having finished another clinical study within the last 4 weeks before inclusion
  • Hypersensitivity, allergy, or intolerance against any compound of the test products (e. g. eggs)
  • Recent implantation of a cardiac pacemaker or other active implants
  • History of or present liver deficiency as defined by Quick \< 70%
  • History of hepatitis B, C, HIV
  • Subjects who are scheduled to undergo any diagnostic intervention or hospitalization which may cause protocol deviations
  • Simultaneous study participation by members of the same household
  • Any diet to lose body weight
  • Eating disorders or vegan diet
  • Present drug abuse or alcoholism

Key Trial Info

Start Date :

June 19 2023

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

November 1 2023

Estimated Enrollment :

40 Patients enrolled

Trial Details

Trial ID

NCT06021665

Start Date

June 19 2023

End Date

November 1 2023

Last Update

March 20 2024

Active Locations (1)

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Citruslabs

Santa Monica, California, United States, 90404