Phase 3Completed

A Prospective, Multi-center Study to Evaluate the Efficacy and Safety of Vitamin D3 B.O.N. Intramuscular Injection in Adults With Vitamin D Deficiency

A Prospective, Multi-centre, Randomized, Double-blind, Placebo-controlled Phase 3 Study to Evaluate the Efficacy and Safety of Vitamin D3 B.O.N. Intramuscular Injection in Adults With Vitamin D Deficiency

Sponsor
Kwang Dong Pharmaceutical co., ltd. (Industry)
Enrolment
84 enrolled
Conditions
Vitamin D Deficiency
Interventions
Vitamin D3 B.O.N. Injection (cholecalciferol 200,000IU); Placebo
Ages
adults, older adults
Registry
NCT02443246

Full record on ClinicalTrials.gov

From the registry

To compare the efficacy of Vitamin D3 B.O.N. Intramuscular Injection within 12 weeks with that of placebo in adults with Vitamin D Deficiency.

Primary outcomes

  • Primary Efficacy Endpoints (serum 25(OH)D concentration)

History

  1. Last registry update

  2. Study completion

  3. Primary completion

  4. Registered

  5. Started