Trial Review

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Trial registered on ANZCTR


Registration number
ACTRN12617000570381
Ethics application status
Approved
Date submitted
12/04/2017
Date registered
24/04/2017
Date last updated
28/10/2021
Date data sharing statement initially provided
28/10/2021
Type of registration
Prospectively registered

Titles & IDs
Public title
Building bone from blood: The effect of vitamin D on circulating bone-forming cells
Scientific title
A randomised, double blind, placebo-controlled trial to determine the effect of vitamin D supplementation on the number of Circulating Osteo-Progenitor (COP) cells in vitamin D-deficient individuals
Secondary ID [1] 291686 0
None
Universal Trial Number (UTN)
U1111-1195-4316
Trial acronym
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Vitamin D deficiency 302973 0
Condition category
Condition code
Musculoskeletal 302441 302441 0 0
Other muscular and skeletal disorders

Intervention/exposure
Study type
Interventional
Description of intervention(s) / exposure
After randomisation, on day 1 of the 3 month dosing period, participants will be given either loading dose of one tablet containing 50000IU of vitamin D orally (treated group - Arm 1) or a tablet containing placebo (placebo group - Arm 2). Both groups will also receive 1000IU/day of vitamin D for 3 months starting on day 1 post-loading dose for both groups. Participants will be required to return every 4 weeks for a total of 3 monthly visits. During each monthly visit, adherence will be monitored by asking the participants to bring their empty bottles of vitamin D tablets. At their monthly visits, participants will receive enough vitamin D tablets (1,000 IU/tablet) for a month. In addition, a monthly blood test (40ml) will be performed.
Intervention code [1] 297771 0
Treatment: Drugs
Comparator / control treatment
Arm 2 will consist of placebo (tablets containing microcrystalin cellulose) followed by 1000IU/day of vitamin D for 3 months, which will be started on day 1 post-loading dose.
Control group
Placebo

Outcomes
Primary outcome [1] 301745 0
The primary outcome of the intervention will be the proportion of participants with an increase in number of circulating osteoprogenitor cells (COP) cells (as a percentage), measure by flow cytometry, at the end of the first month post-loading dose.
Timepoint [1] 301745 0
One month post-loading dose (50,000 IU) of vitamin D
Secondary outcome [1] 333757 0
The secondary outcome would be to observe the rate of increase (monthly) of COP cells for three months. Percentage of COP cells in the circulation will be mesured monthly by flow cytometry.
Timepoint [1] 333757 0
At 1, 2 and 3 months post-loading dose

Eligibility
Key inclusion criteria
1- Age > 55yo
2- Both male and females
3- Independent in Activities of Daily Living (ADL) (Barthel > 60%)
4- Vitamin D deficient < 35 nmol/L
5- Normal Bone Mineral Density (BMD) (>-1 SD)
Minimum age
55 Years
Maximum age
No limit
Sex
Both males and females
Can healthy volunteers participate?
No
Key exclusion criteria
1- Current smoker
2- High Body Mass Index (>30)
3- Diabetics
4- Hematopoietic / Hematological diseases
5- Current or prior use of drugs that could interfere with bone mass (ie Glucocorticosteroids, anti-resorptive drugs, Hormone Replacement Therapy, Teriparatide)
6- History of recent / traumatic fractures in the last 3 months
7- History of bone tumours
8- Aortic valve calcification
9- HyperPTH (>6.8pmol/L)
10- Abnormal thyroid function (Thyroid Stimulating Hormone (TSH) > 10mIU/L)
11- Estimated Glomerular Filtration rate (eGFR) < 35 ml/min

Study design
Purpose of the study
Treatment
Allocation to intervention
Randomised controlled trial
Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Randomisation is achieved at the pharmacy through central randomisation by computer.
Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Simple randomisation using a randomisation table created by computer software (i.e. computerised sequence generation).
Masking / blinding
Blinded (masking used)
Who is / are masked / blinded?
The people receiving the treatment/s
The people administering the treatment/s
The people assessing the outcomes
The people analysing the results/data
Intervention assignment
Parallel
Other design features
Phase
Phase 4
Type of endpoint/s
Efficacy
Statistical methods / analysis
Sample size calculations were based on COP levels observed in healthy populations from previous unpublished datasets. Since COP cells are not normally distributed, the mean and SD of logarithmic transformation will be used (mean -0.9, SD 0.9). It is expected that the intervention group will reach normal COP values within 1 month, while the placebo group will be 50% lower in value. Based on this estimate and assuming a two-tailed significance level of 0.05 and power of 80%, 42 patients per group will be required. Sample size calculations were obtained using STATA 13.0.
Withdrawn participants will not be replaced in the study. Every patient will be contacted and reminded prior to their monthly visits, therefore the drop-out is not expected to exceed 5%. The total number of patients recruited will therefore be 84
All the results will be presented following CONSORT guidelines. Baseline characteristics will be presented as frequencies with percentages and median values with interquartile ranges. The outcome variable will be transformed to follow normal distribution if required. Primary outcome (the difference in COP levels at 1 month) will be analysed on intention to treat principle with case-wise deletion of those patients with missing primary outcome. Statistical test used will be 2-samples independent t-test with no adjustment for covariates (two-tailed level of significance at 5%). Secondary outcomes (the difference in COP levels at 2 and 3 months) will be analysed in similar manner. As part of sensitivity analysis for primary and secondary outcomes, the ‘per-protocol’ analysis will be performed as well as adjustment for unbalanced baseline covariates using linear regression. Missing data imputation will not be attempted unless a large proportion of missing data or its non-random nature is observed during the study and at analysis stage in which case missing data imputation may be performed and results presented as part of sensitivity analysis.

Recruitment
Recruitment status
Stopped early
Data analysis
Data analysis is complete
Reason for early stopping/withdrawal
Participant recruitment difficulties
Other reasons/comments
Other reasons
COVID-19
Date of first participant enrolment
Anticipated
1/07/2018
Actual
1/07/2019
Date of last participant enrolment
Anticipated
28/02/2019
Actual
3/02/2020
Date of last data collection
Anticipated
31/05/2019
Actual
Sample size
Target
84
Accrual to date
Final
18
Recruitment in Australia
Recruitment state(s)
VIC
Recruitment hospital [1] 7836 0
Footscray Hospital - Footscray
Recruitment hospital [2] 7837 0
Sunshine Hospital - St Albans
Recruitment hospital [3] 7838 0
Williamstown Hospital - Williamstown
Recruitment postcode(s) [1] 15774 0
3011 - Footscray
Recruitment postcode(s) [2] 15775 0
3021 - St Albans
Recruitment postcode(s) [3] 15776 0
3016 - Williamstown

Funding & Sponsors
Funding source category [1] 296185 0
University
Name [1] 296185 0
The University of Melbourne
Country [1] 296185 0
Australia
Primary sponsor type
Hospital
Name
Western Health
Address
176 Furlong Road
St. Albans VIC 3021
Country
Australia
Secondary sponsor category [1] 295095 0
None
Name [1] 295095 0
None
Address [1] 295095 0
Country [1] 295095 0

Ethics approval
Ethics application status
Approved
Ethics committee name [1] 297428 0
MELBOURNE HEALTH HUMAN RESEARCH ETHICS COMMITTEE
Ethics committee address [1] 297428 0
Ethics committee country [1] 297428 0
Australia
Date submitted for ethics approval [1] 297428 0
09/12/2016
Approval date [1] 297428 0
10/02/2017
Ethics approval number [1] 297428 0
HREC/16/MH/348

Summary
Brief summary
Trial website
Trial related presentations / publications
Public notes

Contacts
Principal investigator
Name 74006 0
Prof Gustavo Duque
Address 74006 0
Level 3 WCHRE, Sunshine Hospital
176 Furlong Road
St. Albans VIC 3021
Country 74006 0
Australia
Phone 74006 0
+61 3 83958121
Fax 74006 0
Email 74006 0
[email protected]
Contact person for public queries
Name 74007 0
Elizabeth Liberts
Address 74007 0
Level 3 WCHRE, Sunshine Hospital
176 Furlong Road
St. Albans VIC 3021
Country 74007 0
Australia
Phone 74007 0
+61 3 83958121
Fax 74007 0
Email 74007 0
[email protected]
Contact person for scientific queries
Name 74008 0
Karin du Plessis
Address 74008 0
Level 3 WCHRE, Sunshine Hospital
176 Furlong Road
St. Albans VIC 3021
Country 74008 0
Australia
Phone 74008 0
+61 3 83958121
Fax 74008 0
Email 74008 0
[email protected]

Data sharing statement
Will individual participant data (IPD) for this trial be available (including data dictionaries)?
No
No/undecided IPD sharing reason/comment


What supporting documents are/will be available?

No Supporting Document Provided



Results publications and other study-related documents

Documents added manually
No documents have been uploaded by study researchers.

Documents added automatically
No additional documents have been identified.