Melatonin-Micronutrients for Osteopenia Treatment Study (MOTS)
Primary Purpose
Osteoporosis, Osteopenia
Status
Completed
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
Fiber Pill
Melatonin, Strontium citrate, Vitamins D3 and K2
Sponsored by
About this trial
This is an interventional treatment trial for Osteoporosis focused on measuring Melatonin, Strontium Citrate, Osteoporosis, Osteopenia
Eligibility Criteria
Inclusion Criteria:
- postmenopausal
- must be osteopenic (T-score between -2.5 and -1)
- willingness to participate in the 12-month study
- willingness to undergo testing of bone turnover markers before and after the drug therapies
- willingness to provide a self-assessment on quality of life throughout the program
- willingness to take their treatments right before bed
- willingness to not to consume alcohol with this medication
Exclusion Criteria:
- women in whom osteopenia is a result of some other known process (e.g. hyperparathyroidism, metastatic bone disease, multiple myeloma or chronic steroid use).
- women on osteoporotic drugs, hypnotics, CYP1A2 inhibiting drugs, fluvoxamine
- women with severe sleep apnea, severe COPD and those with moderate or severe hepatic or renal impairment.
Sites / Locations
- Duquesne University Center for Pharmacy Care
Arms of the Study
Arm 1
Arm 2
Arm Type
Placebo Comparator
Active Comparator
Arm Label
Fiber pill
strontium/melatonin/Vitamins K2 and D3
Arm Description
2 plant fiber pills taken p.o. (by mouth) nightly for one year
2 pills taken p.o. (by mouth) nightly for one year. Each pill contains strontium citrate (225 mg), melatonin (2.5 mg), Vitamin K2 (MK7) (30 mcg) and Vitamin D3 (1000 IU)
Outcomes
Primary Outcome Measures
Changes in bone mineral density from baseline to one year following treatment
Secondary Outcome Measures
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT01870115
Brief Title
Melatonin-Micronutrients for Osteopenia Treatment Study
Acronym
MOTS
Official Title
Phase 1 Study of Combination Strontium, Melatonin and Nutritional Co-factors on Bone Health and Quality of Life in Postmenopausal Women With Osteopenia
Study Type
Interventional
2. Study Status
Record Verification Date
February 2017
Overall Recruitment Status
Completed
Study Start Date
August 2013 (undefined)
Primary Completion Date
February 9, 2017 (Actual)
Study Completion Date
February 9, 2017 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Duquesne University
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
The investigators' long-term goal is to employ novel methods to improve bone formation and bone density in women (and men) with osteopenia or osteoporosis while also decreasing signs and symptoms of degenerative joint and disc disease that commonly accompany bone loss as well as improve quality of life (QOL). These conditions generally begin silently as early as the menopause transition and progress to osteopenia and osteoporosis during the post-menopausal years in aging women. The investigators also envision this will be beneficial in aging andropausal men with these conditions. The investigators postulate that melatonin in novel combination with other natural bone-protective agents may act in a "chronosynergy" manner to prevent and correct these perturbations, reducing the risk of bone fractures, and lessening the stiffness and pain associated with bone, joint and cartilage degeneration and improving quality of life (QOL). The objective here, which is the investigators' next step in pursuit of our goal, is to assess the efficacy of an alternative therapy that uses a novel combination of bone-forming agents, melatonin, strontium (citrate)/ vitamin K2 (MK7), and vitamin D3 on bone health in a postmenopausal population. Melatonin is a novel alternative to current treatment(s) because it has multiple bone-protective and sleep-promoting activities within the body, and it is relatively safe so it can be used in an aging population without untoward side effects; strontium and vitamin D3 are shown to enhance bone mineralization and improve post-menopausal osteoporosis. The project goal is to identify if this combination therapy improves bone health and QOL compared to women taking placebo. The investigators' central hypothesis is that combination therapy using melatonin, strontium, vitamin K2, and vitamin D3 will improve bone health and overall QOL in postmenopausal women not taking this regimen by reducing osteoclast activity and increasing osteoblast activity and by improving subjective measures of stress, anxiety, depression and menopause-related symptoms.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Osteoporosis, Osteopenia
Keywords
Melatonin, Strontium Citrate, Osteoporosis, Osteopenia
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Parallel Assignment
Model Description
Melatonin (5mg), strontium (citrate; 450mg) vitamin D3 (2000IU)and vitamin K2 (MK7; 60mcg)
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
23 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Fiber pill
Arm Type
Placebo Comparator
Arm Description
2 plant fiber pills taken p.o. (by mouth) nightly for one year
Arm Title
strontium/melatonin/Vitamins K2 and D3
Arm Type
Active Comparator
Arm Description
2 pills taken p.o. (by mouth) nightly for one year. Each pill contains strontium citrate (225 mg), melatonin (2.5 mg), Vitamin K2 (MK7) (30 mcg) and Vitamin D3 (1000 IU)
Intervention Type
Dietary Supplement
Intervention Name(s)
Fiber Pill
Intervention Description
This fiber pill has been manufactured to mimic the pill that contains the dietary supplements melatonin (M), strontium citrate (S), vitamin D3 (D) and vitamin K2 (K) in appearance but does not contain the supplements
Intervention Type
Dietary Supplement
Intervention Name(s)
Melatonin, Strontium citrate, Vitamins D3 and K2
Intervention Description
Each pill has been manufactured to contain the dietary supplements 2.5mg melatonin (M), 225mg strontium citrate (S), 1000IU vitamin D3 (D) and 30mcg vitamin K2 (K)
Primary Outcome Measure Information:
Title
Changes in bone mineral density from baseline to one year following treatment
Time Frame
One year
10. Eligibility
Sex
Female
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
postmenopausal
must be osteopenic (T-score between -2.5 and -1)
willingness to participate in the 12-month study
willingness to undergo testing of bone turnover markers before and after the drug therapies
willingness to provide a self-assessment on quality of life throughout the program
willingness to take their treatments right before bed
willingness to not to consume alcohol with this medication
Exclusion Criteria:
women in whom osteopenia is a result of some other known process (e.g. hyperparathyroidism, metastatic bone disease, multiple myeloma or chronic steroid use).
women on osteoporotic drugs, hypnotics, CYP1A2 inhibiting drugs, fluvoxamine
women with severe sleep apnea, severe COPD and those with moderate or severe hepatic or renal impairment.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Paula A Witt-Enderby, PhD
Organizational Affiliation
Duquesne University
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Mark Swanson, ND
Organizational Affiliation
Private Practice
Official's Role
Principal Investigator
Facility Information:
Facility Name
Duquesne University Center for Pharmacy Care
City
Pittsburgh
State/Province
Pennsylvania
ZIP/Postal Code
15282
Country
United States
12. IPD Sharing Statement
Plan to Share IPD
No
Available IPD and Supporting Information:
Available IPD/Information Type
Publication
Available IPD/Information URL
http://www.aging-us.com/article/101158
Learn more about this trial
Melatonin-Micronutrients for Osteopenia Treatment Study
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