A study to compare the effectiveness and safety of an oral low dose and megadose of cholecalciferol treatment in participants with vitamin D deficiency - a real-life comparison pilot study.

Phase 4

Recruiting

• Conditions: Vitamin D deficiency; Diet and Nutrition - Other diet and nutrition disorders

• Registration Number: ACTRN12607000338460
• Lead Sponsor: Prof. Peter Ebeling

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2007-06-26
• Last Update Posted: 13 January 2020

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 60

Inclusion Criteria

Serum 25(0H) concentration < 50 nmol/L and ability to consent to trial participation.

Exclusion Criteria

Inability to either give informed consent or complete the three month study, primary or tertiary hyperparathyroidism or other causes of hypercalcaemia.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
ormalisation of serum 25(0H) concentrations to > 50 nmol/L[At 3 months]

Secondary Outcome Measures

Name	Time	Method
Safety parameters - serum and urine calcium concentrations.[Serum calcium concentrations will be measured at 10 days and 3 months. 24-hour urine calcium concentrations will be measured at 3 months.]