Isoflavone Treatment for Postmenopausal Osteopenia.
Primary Purpose
Osteopenia, Osteoporosis
Status
Unknown status
Phase
Not Applicable
Locations
Denmark
Study Type
Interventional
Intervention
Red clover extract
Supplementation (placebo)
Sponsored by
About this trial
This is an interventional treatment trial for Osteopenia focused on measuring Aglycones, Isoflavones, Red clover, Osteopenia, Menopause, Bone turnover, Bone mineral density
Eligibility Criteria
Inclusion criteria:
- Age 50-85 years, only women
- Have osteopenia (T score between -1 and -2.5)
- Body Mass Index (BMI) between 20 and 40
Exclusion criteria:
- Taken specific osteoporosis drugs (i.e. bisphosphonates, PTH, estrogen or strontium ranelate) in the past 3 months
- Taken other selective estrogen receptor modulator preparations (raloxifene, tamoxifen or isoflavones) in the past 3 months
- Participation in other clinical trials within the last 3 months
- Previous history of cardiovascular, psychiatric, neurological, and / or kidney disease
- Alcohol or substance abuse or acute illness
- Blood pressure> 160/110
- Pregnant and breastfeeding women
Sites / Locations
- Aarhus University Hospital
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Placebo Comparator
Arm Label
Red clover extract
Placebo group
Arm Description
Group recieving daily red clover extract containing isoflavones (80 mg/d), along with calcium (1040 mg/d), vitamin D (25µg/d) and magnesium (487mg/d).
Group recieving daily placebo extract (with no isoflavone content), calcium (1040 mg/d), vitamin D (25µg/d) and magnesium (487mg/d).
Outcomes
Primary Outcome Measures
Plasma C-terminal telopeptide (CTX)
Bone mineral resorption biomarker.
Secondary Outcome Measures
Bone mineral density via dual energy X-ray absorptiometry
Objective measure of bone mineral density and bone mineral content.
Full Information
NCT ID
NCT02174666
First Posted
June 19, 2014
Last Updated
December 14, 2015
Sponsor
University of Aarhus
Collaborators
European Regional Development Fund, The Ministry of Science, Technology and Innovation, Denmark
1. Study Identification
Unique Protocol Identification Number
NCT02174666
Brief Title
Isoflavone Treatment for Postmenopausal Osteopenia.
Official Title
The Effects of Red Clover Treatment on Bone Tissue Regulation in Postmenopausal Osteopenia.
Study Type
Interventional
2. Study Status
Record Verification Date
December 2015
Overall Recruitment Status
Unknown status
Study Start Date
June 2014 (undefined)
Primary Completion Date
June 2016 (Anticipated)
Study Completion Date
September 2016 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Aarhus
Collaborators
European Regional Development Fund, The Ministry of Science, Technology and Innovation, Denmark
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The aim of the project is to execute a double-blind, parallel, randomized 12-month intervention trial on postmenopausal women with osteopenia (low bone mineral density), in order to determine the effects of daily intake of fermented red clover (RC) extract on estrogen dependent bone mineral resorption when compared to placebo. Both groups will recieve equivalent daily calcium, vitamin D and magnesium supplements. The project will also assess whether bioactive compounds in RC can reduce the risk of developing cardiovascular disease.
Detailed Description
The project aims to determine whether red clover derived isoflavones have capabilities to exert positive effects in conditions of osteoporosis and osteopenia in states estrogen deficiency and/or dysregulation.
The cause of osteopenia in women is thought to arise from the deficiency of and/or dysregulation by estrogen on target tissues. Hormone Replacement Therapy (HRT) has proven to be an effective treatment, however it retains limited use as there is general consensus that it also increases cancer risk. Plant derived compounds that emulate the chemical structure and behaviour of estrogen (known as isoflavones) offer a compelling alternative to HRT, due to their potential to adopt the regulatory roles of estrogen without incurring equivalent negative side effects of HRT.
There are, at present, few or no direct head to head clinical trials assessing combination treatments of isoflavones, vitamin D and calcium in contrast to standard vitamin D and calcium supplementation proscribed to osteopenic patients. Research in this area will therefore provide valuable insight into the effectiveness of isoflavones to reduce resorption and/or to stimulate the formation of bone tissue. Moreover the study will provide a comprehensive assessment of the potential of isoflavones to enhance the efficacy of existing preventative treatments. Outcomes of the project have the prospect to help thousands of middle aged and PM women suffering. Moreover, the project may enable development of functional foods and/or nutraceuticals that can be used as either a preventative measure and/or as a treatment for osteoporosis in states of estrogen deficiency and thereby provide an alternative to Hormone Replacement Therapy that does involve the same side effects and risks.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Osteopenia, Osteoporosis
Keywords
Aglycones, Isoflavones, Red clover, Osteopenia, Menopause, Bone turnover, Bone mineral density
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
87 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Red clover extract
Arm Type
Active Comparator
Arm Description
Group recieving daily red clover extract containing isoflavones (80 mg/d), along with calcium (1040 mg/d), vitamin D (25µg/d) and magnesium (487mg/d).
Arm Title
Placebo group
Arm Type
Placebo Comparator
Arm Description
Group recieving daily placebo extract (with no isoflavone content), calcium (1040 mg/d), vitamin D (25µg/d) and magnesium (487mg/d).
Intervention Type
Dietary Supplement
Intervention Name(s)
Red clover extract
Other Intervention Name(s)
Formononetin, Biochanin A, Genistein, Daidzein, Vitamin D, Magnesium, Calcium
Intervention Description
Aglycone isoflavones 80mg/d
Intervention Type
Dietary Supplement
Intervention Name(s)
Supplementation (placebo)
Other Intervention Name(s)
Vitamin D, Magnesium, Calcuim
Primary Outcome Measure Information:
Title
Plasma C-terminal telopeptide (CTX)
Description
Bone mineral resorption biomarker.
Time Frame
0 - 12 months
Secondary Outcome Measure Information:
Title
Bone mineral density via dual energy X-ray absorptiometry
Description
Objective measure of bone mineral density and bone mineral content.
Time Frame
0 - 12 months
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
50 Years
Maximum Age & Unit of Time
85 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion criteria:
Age 50-85 years, only women
Have osteopenia (T score between -1 and -2.5)
Body Mass Index (BMI) between 20 and 40
Exclusion criteria:
Taken specific osteoporosis drugs (i.e. bisphosphonates, PTH, estrogen or strontium ranelate) in the past 3 months
Taken other selective estrogen receptor modulator preparations (raloxifene, tamoxifen or isoflavones) in the past 3 months
Participation in other clinical trials within the last 3 months
Previous history of cardiovascular, psychiatric, neurological, and / or kidney disease
Alcohol or substance abuse or acute illness
Blood pressure> 160/110
Pregnant and breastfeeding women
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Per B Jeppesen, Prof PhD
Organizational Affiliation
Department of Medicine and Endocrinology MEA, Aarhus University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Aarhus University Hospital
City
Aarhus
State/Province
Central Jutland Region
ZIP/Postal Code
8000
Country
Denmark
12. IPD Sharing Statement
Citations:
PubMed Identifier
28768651
Citation
Lambert MNT, Thybo CB, Lykkeboe S, Rasmussen LM, Frette X, Christensen LP, Jeppesen PB. Combined bioavailable isoflavones and probiotics improve bone status and estrogen metabolism in postmenopausal osteopenic women: a randomized controlled trial. Am J Clin Nutr. 2017 Sep;106(3):909-920. doi: 10.3945/ajcn.117.153353. Epub 2017 Aug 2.
Results Reference
derived
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Isoflavone Treatment for Postmenopausal Osteopenia.
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