Osteoarthritis Clinical Trial
Official title:
A Single Arm Pilot Study to Evaluate the Effectiveness of Eggshell Membrane Compositions for the Treatment of Pain Associated With Connective Tissue and Joints
| NCT number | NCT00750230 |
| Other study ID # | CLN# A0803 |
| Secondary ID | |
| Status | Completed |
| Phase | N/A |
| First received | |
| Last updated | |
| Start date | October 2003 |
| Est. completion date | January 2004 |
| Verified date | February 2016 |
| Source | ESM Technologies, LLC |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | |
| Study type | Interventional |
The purpose of this study was to evaluate the use of the dietary supplement Natural Eggshell Membrane (NEM) for the treatment of joint and connective tissue discomfort, pain, and flexibility.
| Status | Completed |
| Enrollment | 11 |
| Est. completion date | January 2004 |
| Est. primary completion date | December 2003 |
| Accepts healthy volunteers | No |
| Gender | All |
| Age group | 18 Years to 100 Years |
| Eligibility | Inclusion Criteria: - patients seeking relief of mild to moderate pain due to joint or connective tissue (JCT)disorders. - subjects must have had persistent pain associated with a JCT disorder. - subjects were required to suspend all current pain relief medications. - Subjects that were currently taking analgesic medications were eligible to participate in the studies following a 14 day washout period for NSAIDs, a 7 day washout for narcotics, and a 90 day washout for injected steroids. - subjects currently taking glucosamine, chondroitin sulfate or MSM were only eligible after a 3-month washout period. Exclusion Criteria: - Patients were excluded if they were currently receiving remission-inducing drugs such as methotrexate or immunosuppressive medications or had received them within the past 3 months. - body weight 250 pounds or greater. - a known allergy to eggs or egg products. - pregnant or breastfeeding women. - subjects previously enrolled in a study to evaluate pain relief within the past 6 months or currently involved in any other research study involving an investigational product (drug, device, or biologic) or a new application of an approved product, within 30 days of screening. |
| Country | Name | City | State |
|---|---|---|---|
| United States | Robinson Family Clinic | Carthage | Missouri |
| Lead Sponsor | Collaborator |
|---|---|
| ESM Technologies, LLC |
United States,
Ruff KJ, DeVore DP, Leu MD, Robinson MA. Eggshell membrane: a possible new natural therapeutic for joint and connective tissue disorders. Results from two open-label human clinical studies. Clin Interv Aging. 2009;4:235-40. doi: 10.2147/cia.s5797. Epub 20 — View Citation
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | The primary outcome measure of this study was to evaluate the mean effectiveness of NEM® in relieving general pain associated with moderate joint & connective tissue disorders. | 7 & 30 days | ||
| Secondary | Additional outcome measures were to evaluate flexibility | 7 & 30 days | ||
| Secondary | Secondary objectives of the study were to evaluate tolerability and any adverse reactions associated with supplementation with NEM®. | 7 & 30 days | ||
| Secondary | To evaluate pain associated with the range of motion (ROM) evaluation. | 7 & 30 days |
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