CompletedPhase 3NCT02069990

Controlled, Randomized, Four-arm Comparative, Open Label, Multi-centric Clinical Trial to Compare the Efficacy and Safety Parameters of the Once-a-week or Once-a-month Administered 7000 IU, or 30000 IU Vitamin D (Cholecalciferol) to a 1000 IU Dosage Applied Daily in Vitamin D Deficient Patients

Studying Disorders of vitamin D metabolism

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Key facts

Sponsor
Semmelweis University
Principal Investigator
Peter Lakatos, professor
Semmelweis University
Intervention
Cholecalciferol(drug)
Enrollment
89 target
Eligibility
18 years · All sexes
Timeline
20132013

Study locations (2)

Collaborators

Pharma Patent Kft.

Primary source

Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.

Open NCT02069990 on ClinicalTrials.gov

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