drugset / Trial / NCT02457247

Calcichew D3 Preference Study in Participants Eligible for Calcium and Vitamin D Supplementation.

NCT02457247 ↗

Phase 4 Completed 276 enrolled Takeda
RandomizedCrossoverOpen-labelTreatment

Summary

The purpose of this study is to compare the preference of Calcichew D3 500/400 (containing 500 mg calcium and 400 IU of vitamin D) with Adcal-D3 600/400 (containing 600 mg of calcium and 400 IU of vitamin D) in Test Group 1, and to compare Calcichew D3 500/800 (containing 500 mg calcium and 800 IU vitamin D) with Kalcipos-D 500/800 (containing 500 mg of calcium and 800 IU of vitamin D) in Test Group 2.

Timeline

Start
2015-06
Primary completion
2015-08
Completion
2015-08

Outcome

Met primary endpoint

paper Calcichew 500/400 (77.6%) over Adcal-D3 was 3.46 ([95% CI 2.24, 5.36], p < 0.001) in Group 1 PMID 27322906 ↗

paper Calcichew D3 500/800 (63.2%) over Kalcipos-D was 1.72 ([1.19, 2.47], p = 0.004) in Group 2 PMID 27322906 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Adcal-D3 Unknown 400 iu Oral
Subject Adcal-D3 Unknown 600 mg Oral
Subject Calcichew D3 Unknown 400 iu —
Subject Calcichew D3 Unknown 500 mg —
Subject Calcichew D3 Unknown 800 iu —
Subject Kalcipos-D Unknown 500 mg Oral
Subject Kalcipos-D Unknown 800 iu Oral

Indications