Vitamin K Supplementation in Post-Menopausal Osteopenia

Post-Menopausal Osteoporosis Clinical Trial

Official title:

Evaluation of the Clinical Use of Vitamin K Supplementation in Post-Menopausal Women With Osteopenia (ECKO Trial)

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00150969
• Other study ID #: 01-0169
• Secondary ID: 50422
• Status: Completed
• Phase: Phase 3
• Start date: January 2002
• Est. completion date: September 2007

Study information

• Verified date: December 2023
• Source: University Health Network, Toronto
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of this study is to determine whether supplementation with 5 mg vitamin K daily over a 2-year period will prevent bone loss in post-menopausal women with osteopenia.

Description:

Osteoporosis is major cause of morbidity and mortality in Canadian postmenopausal women. It is a systemic disease characterized by low bone mass and deterioration of bone microarchitecture, resulting in bone fragility and an increased risk of fractures. One in six women over the age of 50 have osteoporosis. The lifetime risk of an osteoporotic fracture for an average 50 year-old Canadian woman is >40%. The annual health care costs for osteoporotic fractures in Canada have been estimated to exceed $1.3 billion.

Recent data suggest that vitamin K supplements may decrease bone loss and prevent fractures. Vitamin K is a co-factor of gamma-glutamyl carboxylase, an enzyme that catalyzes the gamma-carboxylation of glutamic acid residues in bone matrix proteins such as osteocalcin. Vitamin K has been reported to enhance bone formation in both in vitro studies and in vivo studies in animals. Vitamin K levels are low in individuals with osteoporosis and in patients with osteoporotic fractures. The few studies examining vitamin K supplementation in humans have showed promising results with no significant side effects, but these studies had significant methodological shortcomings such as inadequate sample size and lack of randomization.

The primary objective of our study is to examine whether vitamin K supplementation will increase bone mineral density in postmenopausal women with osteopenia. Our secondary objectives are to examine the possible adverse effects from long-term vitamin K supplementation, to investigate whether vitamin K will decrease risk of fractures and to determine if vitamin K affects quality of life. Our hypotheses are that vitamin K increases bone mineral density in postmenopausal women, and that there are no significant adverse effects from vitamin K supplementation.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 440
• Est. completion date: September 2007
• Est. primary completion date: September 2006
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Female
• Age group: 18 Years to 100 Years

Eligibility

Inclusion Criteria:

Postmenopausal: One year since the natural cessation of menses, or Hysterectomy with either postmenopausal status confirmed by FSH lab values, or age 55 and above AND 2. Osteopenic: T-score at baseline has to be between (and including) -1.0 and

-2.0 in the lumbar spine (L1-L4), total hip or femoral neck, and the lowest reading of the above three measurements must be between -1.0 and -2.0

Exclusion Criteria:

1. Women ever having had a fragility fracture after age 40;

2. Women currently on anticoagulants, previously on anticoagulants in the past 3 months, or expected to be on anticoagulants in the near future;

3. Women on hormone replacement therapy, raloxifene, bisphosphonates or calcitonin during the past 3 months;

4. Women who have ever been on a bisphosphonate for more than 6 months;

5. Women previously diagnosed with Paget's disease, hyperparathyroidism, hyperthyroidism or other metabolic bone diseases;

6. Women with decompensated diseases of the liver, kidney, pancreas, lung, or heart;

7. Women with a history of active cancer in the past 5 years;

8. Women taking mega-doses of vitamin A (more than 10,000 iu per day) or E (more than 400 iu per day);

9. Women involved in other clinical trials;

10. Any women who, in the opinion of the principal investigator, is at poor medical or psychiatric risk for the study.

Related Conditions & MeSH terms

• Bone Diseases, Metabolic
• Osteoporosis
• Osteoporosis, Postmenopausal
• Post-Menopausal Osteopenia
• Post-Menopausal Osteoporosis

Intervention

Dietary Supplement:
• vitamin K1 (phylloquinone)

• placebo
1 pill daily

Locations

Country	Name	City	State
Canada	Mt. Sinai Hospital	Toronto	Ontario
Canada	St. Michael's Hospital Health Centre	Toronto	Ontario
Canada	Sunnybrook & Women's College Health Sciences Centre	Toronto	Ontario
Canada	University Health Network, Osteoporosis Department	Toronto	Ontario
Canada	University of Toronto	Toronto	Ontario

Sponsors (2)

Lead Sponsor	Collaborator
University Health Network, Toronto	Canadian Institutes of Health Research (CIHR)

Country where clinical trial is conducted

Canada, 

References & Publications (1)

Cheung AM, Tile L, Lee Y, Tomlinson G, Hawker G, Scher J, Hu H, Vieth R, Thompson L, Jamal S, Josse R. Vitamin K supplementation in postmenopausal women with osteopenia (ECKO trial): a randomized controlled trial. PLoS Med. 2008 Oct 14;5(10):e196. doi: 10 — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Percent Change in Bone Mineral Density (BMD) at the Lumbar Spine (L1-L4) Between Treatment Arms.	BMD was measured yearly on one scanner at UHN using DEXA Hologic 4500A densitometer	0 to 24 months
Primary	Percent Change in Bone Mineral Density (BMD) at the Total Hip Between Treatment Arms.	BMD was measured yearly on one scanner at UHN using DEXA Hologic 4500A densitometer	0 to 24 months
Secondary	Percent Change in Bone Mineral Density (BMD) at the Femoral Neck Between Treatment Arms.	BMD was measured yearly on one scanner at UHN using DEXA Hologic 4500A densitometer	0 to 24 months
Secondary	Percent Change in Bone Mineral Density (BMD) at the Ultra-distal Radius Between Treatment Arms.	BMD was measured yearly on one scanner at UHN using DEXA Hologic 4500A densitometer	0 to 24 months
Secondary	Effect of Vitamin K1 Supplementation on Levels of Bone Formation Marker	measured by osteocalcin on elecsys platform	0-24 months
Secondary	Effect of Vitamin K1 Supplementation on Level of Bone Resorption Markers (C-telopeptide: CTX)	measured by CTX Elisa assay on elecsys platform	0-24 months
Secondary	Effect of Vitamin K1 Supplementation on Percent of Carboxylation of Osteocalcin	measured by osteocalcin hydroxyapatite binding assay	0 to 24 months
Secondary	Percent Change in Bone Mineral Density (BMD) at the Total Hip Between Treatment Arms.	BMD was measured yearly on one scanner at UHN using DEXA Hologic 4500A densitometer	0 to 48 months
Secondary	Percent Change in Bone Mineral Density (BMD) at the Lumbar Spine (L1-L4) Between Treatment Arms.	BMD was measured yearly on one scanner at UHN using DEXA Hologic 4500A densitometer	0 to 48 months
Secondary	Percent Change in Bone Mineral Density (BMD) at the Femoral Neck Between Treatment Arms.	BMD was measured yearly on one scanner at UHN using DEXA Hologic 4500A densitometer	0 to 48 months
Secondary	Percent Change in Bone Mineral Density (BMD) at the Ultra-distal Radius Between Treatment Arms.	BMD was measured yearly on one scanner at UHN using DEXA Hologic 4500A densitometer	0 to 48 months
Secondary	Difference in Serious Adverse Events	These include hospitalizations for pneumonia, heart failure, gastro-intestinal bleeding, elective and non-elective surgery, cancer and death.	up to 48 months
Secondary	Difference in Number of New Cancers by Treatment Arm.		up to 48 months
Secondary	Difference in Number of New Clinical Fractures by Treatment Arm.	these included fragility fractures	up to 48 months