Status:

COMPLETED

Intervention Study of Vitamin D Supplementation to Prevent Cardiovascular Disease

Lead Sponsor:

Chinese PLA General Hospital

Conditions:

Vitamin D Deficiency

Eligibility:

All Genders

20-90 years

Phase:

NA

Brief Summary

This is a 9 months, randomized, single center, open-label, parallel-group study to compare the efficacy and safety parameters of vitamin D supplementation in vitamin D deficiency subjects in China.

Detailed Description

This is a 9 months, randomized, single center, open-label, parallel-group study to compare the efficacy and safety parameters of vitamin D supplementation in vitamin D deficiency subjects in China. E...

Eligibility Criteria

Inclusion

  • Informed consent obtained before any trial-related activities. (Trial- related activities are any procedure that would not have been performed during normal management of the subject.)
  • 25OHD\<30ng/ml

Exclusion

  • Severe systemic disease (including severe heart, liver, kidney and lung diseases, severe infection, mental disorder and connective tissue disease)
  • Primary hyperparathyroidism, other bone disease, malabsorption and other chronic gastrointestinal disease.
  • Pregnant, breast-feeding or the intention of becoming pregnant or not using adequate contraceptive measures.
  • Use of systemic or inhaled glucocorticoids or other medication known to interfere with bone metabolism.
  • Use of vitamin D related agents in recent 3 months.

Key Trial Info

Start Date :

June 1 2014

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

June 1 2015

Estimated Enrollment :

100 Patients enrolled

Trial Details

Trial ID

NCT03339427

Start Date

June 1 2014

End Date

June 1 2015

Last Update

November 13 2017

Active Locations (1)

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PLA General Hospital

Beijing, Beijing Municipality, China, 100853