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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02822651
Other study ID # 69HCL15_0078
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date September 19, 2016
Est. completion date November 17, 2017

Study information

Verified date December 2018
Source Hospices Civils de Lyon
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Vitamin D has effects on many tissues, and hypovitaminosis D is frequent. In a French survey conducted among 1587 adults, vitamin D insufficiency (<30ng/ml) has been reported in 80% of subjects, including 43% with moderate deficiency (<20ng/ml) and 5% with severe deficiency (<10ng/ml).

Because of the possible consequences of hypovitaminosis D (osteomalacia in adults…), the number of vitamin D determination has increased ten-fold since 2005 in France, reaching 4.5 million € in 2011, and with it the costs for health insurance. However, there is currently no consensus on the strategy for detection, diagnosis and treatment of hypovitaminosis D.

We propose to develop a predictive clinical score of hypovitaminosis D based on the accurate assessment of solar exposure, vitamin D intakes and hypovitaminosis D risk factors collected through a self-administered questionnaire.


Recruitment information / eligibility

Status Completed
Enrollment 2592
Est. completion date November 17, 2017
Est. primary completion date November 17, 2017
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria:

- Men and women aged 18 to 70 years old

Exclusion Criteria:

- Participation in a study related to vitamin D

- Taking at least 80 000 IU vitamin D in the last 3 months as a single dose

- Pregnancy or breast-feeding

- Renal failure : severe renal impairment, dialysis, having kidney transplant

- Known hepatic impairment

- Gastrointestinal disorders: Celiac disease, Crohn's disease, ulcerative colitis, bariatric surgery, gastrointestinal surgery with stoma

- Known primary hypo/hyperparathyroidism

- Bone cancer/metastases current or in the last 2 years

- Treatment with antiepileptics

- Long-term treatment with glucocorticoids (> 3 months)

- Treatment with antiretroviral

- Legal incapacity or limited legal capacity

- Non-recipient of French Social Security

Study Design


Related Conditions & MeSH terms


Intervention

Biological:
Blood sampling
Patients will have a blood sampling at inclusion to measure vitamin D blood concentration.
Other:
self-administered questionnaire
Patients will fill a self-administered questionnaire the day of inclusion

Locations

Country Name City State
France Hospices Civils de Lyon - Pôle IMER Lyon Cedex 03

Sponsors (1)

Lead Sponsor Collaborator
Hospices Civils de Lyon

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary 25 (OH) vitamin D blood concentration Vitamin D determination will be carried out for each center in a single laboratory by chemiluminescence technique.
Vitamin D determination is the gold standard for the development and validation phases of the score. It will define the variables of the self-administered questionnaire to be included in the final score (development phase) and be the gold standard in the evaluation of the performance score (validation phase). The blood sample will be collected after the completion of the questionnaire, on the same day.
The day of inclusion
Secondary Vitamin D concentration level The ability of the score to classify adults in one of these three categories:
Category 1 : Vitamin D sufficiency (=30 ng/ml)
Category 2 : Hypovitaminosis D between 30 and 10 ng/ml
Vitamin D insufficiency (<30 ng/ml)
Vitamin D deficiency (<20 ng/ml)
Category 3 : Severe deficiency (<10 ng/ml)
The day of inclusion
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