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OpenTrials
Completed

NCT Number: NCT04764110

Short-term Impact of Cyplexinol® on Self-reported Joint Pain

In this study, the impact of 900 mg Cyplexinol® taken daily on joint pain over a period of 15 days in comparison with a placebo will be determined using a cross-over double blind design with a 13 day wash out period. In addition, we will measure cytokine production and related variables during the two hour after subjects ingest a single dosage of Cyplexinol® or placebo on days 1 and 15.

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Key information

Age range

30 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Center for Nutraceutical and Dietary Supplement Reseach

Memphis, Tennessee, 38152, United States

About this study

Chronic inflammation can induce joint pain, which is a common problem among adult men and women. ZyCal Bioceuticals is a manufacturer of natural ingredients and finished nutritional supplements to support bone and joint health in humans. The core ingredient in all ZyCal products is Cyplexinol® (a Bone Morphogenetic Protein [BMP] Complex). BMP complexes have been shown to activate mesenchymal stem cells to help the body regenerate osteoblasts and chondrocytes. BMPs were initially identified in the 1970's as osteogenic factors which stimulate activation, proliferation, and differentiation of osteoprogenitor cells by binding BMP receptors and subsequent signaling through the SMAD pathway. BMPs have also been shown to reduce inflammation and promote healthy inflammatory signaling in joints and other tissues.

Cyplexinol® is delivered in the dietary supplement called Ostinol™, which has been safely used in oral form by thousands of people since 2007 for bone and joint health. Currently Cyplexinol® is considered a dietary supplement ingredient and has been awarded GRAS (generally recognized as safe).

Studies have been conducted to evaluate the safety and efficacy of Cyplexinol® as a dietary supplement for joint health (Garian, 2012; Scaffidi, 2017). Dosages of 150mg Cyplexinol® have been compared to a placebo (negative control) alone or in combination with glucosamine /chondroitin in randomized controlled trials for 4 -12 weeks. Endpoints examined have included joint stiffness, inflammation, pain, and overall quality of life. However, to date, no short-term studies have been conducted using Cyplexinol®, nor have any acute studies evaluated the impact of this agent on immune function.

In this study, the impact of 900 mg Cyplexinol® taken daily on joint pain over a period of 15 days in comparison with a placebo will be determined using a cross-over double blind design with a 13 day wash out period. In addition, we will measure cytokine production and related variables during the two hour post ingestion period after subjects ingest a single dosage of Cyplexinol® or placebo on days 1 and 15.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • body mass index (BMI) between 18-29.9 kg/m2 (not obese)
  • no consumption of alcohol-containing beverages within 48 hours of testing
  • experiencing self-reported joint pain with a minimum pain rating of 3/10 for at least the past 30 days
  • engaged in structured exercise 2 or more days per week for the past 6 months or longer
  • a negative verbal pre-study drug screen (alcohol abuse, amphetamines, benzodiazepines, cocaine, opioids, phencyclidine, barbiturates, cotinine), no history of use of illicit drugs or other substances of abuse within 12 months of the screening visit

Exclusion criteria

  • pregnant
  • tobacco user
  • active infection or illness of any kind
  • rheumatic or osteoarthritic diagnosis
  • Using anti-inflammatory medicines, pain medications, or dietary supplements (or not willing to cease for one-month prior to participation and throughout study)

Treatment and study plan

Cyplexinol

Dietary Supplement

partially hydrolyzed Collagen and its associated proteins including Bone Morphogenetic Proteins (BMPs)

Placebo

Other

Maltodextrin

Primary outcomes

  1. TNF-alpha

    Time frame: baseline of day 1

    TNF-alpha measured in blood

  2. TNF-alpha

    Time frame: baseline of day 15

    TNF-alpha measured in blood

  3. TNF-alpha

    Time frame: 60 min after treatment ingestion of day 1

    TNF-alpha measured in blood

  4. TNF-alpha

    Time frame: 60 min after treatment ingestion of day 15

    TNF-alpha measured in blood

  5. TNF-alpha

    Time frame: 120 min after treatment ingestion of day 1

    TNF-alpha measured in blood

  6. TNF-alpha

    Time frame: 120 min after treatment ingestion of day 15

    TNF-alpha measured in blood

  7. IL-6

    Time frame: baseline of day 1

    IL-6 measured in blood

  8. IL-6

    Time frame: baseline of day 15

    IL-6 measured in blood

  9. IL-6

    Time frame: 60 min after treatment ingestion of day 1

    IL-6 measured in blood

  10. IL-6

    Time frame: 60 min after treatment ingestion of day 15

    IL-6 measured in blood

  11. IL-6

    Time frame: 120 min after treatment ingestion of day 1

    IL-6 measured in blood

  12. IL-6

    Time frame: 120 min after treatment ingestion of day 15

    IL-6 measured in blood

  13. IL-10

    Time frame: baseline of day 1

    IL-10 measured in blood

  14. IL-10

    Time frame: baseline of day 15

    IL-10 measured in blood

  15. IL-10

    Time frame: 60 min after treatment ingestion of day 1

    IL-10 measured in blood

  16. IL-10

    Time frame: 60 min after treatment ingestion of day 15

    IL-10 measured in blood

  17. IL-10

    Time frame: 120 min after treatment ingestion of day 1

    IL-10 measured in blood

  18. IL-10

    Time frame: 120 min after treatment ingestion of day 15

    IL-10 measured in blood

  19. IL-1beta

    Time frame: baseline of day 1

    IL-1beta measured in blood

  20. IL-1beta

    Time frame: baseline of day 15

    IL-1beta measured in blood

  21. IL-1beta

    Time frame: 60 min after treatment ingestion of day 1

    IL-1beta measured in blood

  22. IL-1beta

    Time frame: 60 min after treatment ingestion of day 15

    IL-1beta measured in blood

  23. IL-1beta

    Time frame: 120 min after treatment ingestion of day 1

    IL-1beta measured in blood

  24. IL-1beta

    Time frame: 120 min after treatment ingestion of day 15

    IL-1beta measured in blood

  25. osteocalcin

    Time frame: baseline day 1

    osteocalcin measured in blood

  26. osteocalcin

    Time frame: baseline day 15

    osteocalcin measured in blood

  27. osteocalcin

    Time frame: 60 min after treatment ingestion of day 1

    osteocalcin measured in blood

  28. osteocalcin

    Time frame: 60 min after treatment ingestion of day 15

    osteocalcin measured in blood

  29. osteocalcin

    Time frame: 120 min after treatment ingestion of day 1

    osteocalcin measured in blood

  30. osteocalcin

    Time frame: 120 min after treatment ingestion of day 15

    osteocalcin measured in blood

  31. alkaline phosphatase

    Time frame: baseline day 1

    alkaline phosphatase measured in blood

  32. alkaline phosphatase

    Time frame: baseline day 15

    alkaline phosphatase measured in blood

  33. alkaline phosphatase

    Time frame: 60 min after treatment ingestion of day 1

    alkaline phosphatase measured in blood

  34. alkaline phosphatase

    Time frame: 60 min after treatment ingestion of day 15

    alkaline phosphatase measured in blood

  35. alkaline phosphatase

    Time frame: 120 min after treatment ingestion of day 1

    alkaline phosphatase measured in blood

  36. alkaline phosphatase

    Time frame: 120 min after treatment ingestion of day 15

    alkaline phosphatase measured in blood

  37. Bone Morphogenetic Protein

    Time frame: baseline day 1

    Bone Morphogenetic Protein measured in blood

  38. Bone Morphogenetic Protein

    Time frame: baseline day 15

    Bone Morphogenetic Protein measured in blood

  39. Bone Morphogenetic Protein

    Time frame: 60 min after treatment ingestion of day 1

    Bone Morphogenetic Protein measured in blood

  40. Bone Morphogenetic Protein

    Time frame: 60 min after treatment ingestion of day 15

    Bone Morphogenetic Protein measured in blood

  41. Bone Morphogenetic Protein

    Time frame: 120 min after treatment ingestion of day 1

    Bone Morphogenetic Protein measured in blood

  42. Bone Morphogenetic Protein

    Time frame: 120 min after treatment ingestion of day 15

    Bone Morphogenetic Protein measured in blood

  43. Joint pain visual analog scale

    Time frame: Day 1 of treatment

    A 100mm visual analog scale will be used to assess joint pain. Scores range from 0 (subject strongly disagreeing with prompt) to 100 (strongly agree).

  44. Joint pain visual analog scale

    Time frame: Day 15 of treatment

    A 100mm visual analog scale will be used to assess joint pain. Scores range from 0 (subject strongly disagreeing with prompt) to 100 (strongly agree).

  45. Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC)

    Time frame: Day 1 of treatment

    The WOMAC measures five items for pain (score range 0-20), two for stiffness (score range 0-8), and 17 for functional limitation (score range 0-68) with 0 being none and high values being most.

  46. Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC)

    Time frame: Day 15 of treatment

    The WOMAC measures five items for pain (score range 0-20), two for stiffness (score range 0-8), and 17 for functional limitation (score range 0-68) with 0 being none and high values being most.

Secondary outcomes

  1. Dietary intake

    Time frame: Day 1 of treatment

    Dietary intake of subjects for 3-days prior to testing days analyzed using Food Processor Pro software for total calories, macro- and micro-nutrient composition

  2. Dietary intake

    Time frame: Day 15 of treatment

    Dietary intake of subjects for 3-days prior to testing days analyzed using Food Processor Pro software for total calories, macro- and micro-nutrient composition

Sponsors and collaborators

Lead sponsor

University of Memphis

Other

Collaborators

  • ZyCal Bioceuticals

Registry information

Official study title

Short-term Impact of Cyplexinol® on Inflammatory Status and Related Measures in Men and Women With Self-reported Joint Pain

Important dates

Study start
2021
Primary completion
2022
Study completion
2022
First posted
Feb 21, 2021
Registry last updated
Aug 22, 2022

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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