Clinical Trials Directory

Trials / Completed

CompletedNCT01694355

The Impact of Severe Vitamin D Deficiency and Its Correction on Bone Mineral Density (BMD) in Postmenopausal Women

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
32 (actual)
Sponsor
Soroka University Medical Center · Academic / Other
Sex
Female
Age
55 Years – 70 Years
Healthy volunteers
Accepted

Summary

It is well known that postmenopausal women are at risk for osteoporosis. The study hypothesis is that vitamin D deficiency (≤17.5nmol/L) is frequently associated with osteomalacia and will cause low BMD estimation in DXA scan due to insufficient bone mineralization. We assume that among these postmenopausal women, Vitamin D treatment will improve bone mineralization and will cause a rapid increase in BMD. According to the results, bisphosphonates therapy may be an unnecessary treatment. The objective of this study is to evaluate the impact of severe vitamin D deficiency and its correction on Bone Mineral Density (BMD) in postmenopausal women.

Conditions

Interventions

TypeNameDescription
DRUGVitamin D

Timeline

Start date
2012-10-01
Primary completion
2018-10-01
Completion
2018-12-01
First posted
2012-09-27
Last updated
2019-04-05

Locations

1 site across 1 country: Israel

Source: ClinicalTrials.gov record NCT01694355. Inclusion in this directory is not an endorsement.