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Monocentric Randomized Study, Assessing the Interests of the Determination of Vitamin D in Prison Population. (Vitamine D)

C

Centre Hospitalier Departemental Vendee

Status

Completed

Conditions

Male Prisoner

Treatments

Other: Dosage Vitamine D

Study type

Interventional

Funder types

Other

Identifiers

NCT02044133
CHD026-12

Details and patient eligibility

About

The study will be proposed to man entering the prison of La Roche sur Yon. Participants will be randomized into two arms: one arm realize a dosage of vitamin D at the entrance and 6 months after the entry and the second arm will carry only a dosage six months after entry.

the purpose of the study is to determine the interest of dosage of vitamin D in biological assessment of entry into prison house.

Enrollment

54 patients

Sex

Male

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Incarcerated person
  • Imprisoned in La Roche sur Yon
  • Male
  • Age > 18 year old
  • Not opposed to participation in the study

Exclusion criteria

  • Intellectual deficit not to understand the study
  • Taking osteoporosis treatment or any other affecting the metabolism of vitamin D
  • Renal failure, liver failure
  • Hypercalcemia
  • Thyroid dysfunction, parathyroid diseases
  • Duration of imprisonment less than the expected duration of the study.
  • Incarcerated person who had received supplementation of vitamin D in the 6 months prior

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

54 participants in 2 patient groups

Dosage of vitamine D : inclusion and 6 month
Other group
Description:
Participant will have one dosage of vitamine D to entrance of prison and one dosage of vitamine D 6 month after entry
Treatment:
Other: Dosage Vitamine D
Dosage of Vitamine D 6 month
Other group
Description:
Participant will have one dosage of vitamine D 6 month after entry to prison
Treatment:
Other: Dosage Vitamine D

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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