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N/A Completed N=22 Randomized Double-blind Treatment

Treatment of Hypovitaminosis D in Rheumatoid Arthritis

Rheumatoid Arthritis · Hypovitaminosis D
Source: ClinicalTrials.gov NCT00423358 ↗
Enrolled (actual)
22
Serious AEs
0.0%
Results posted
Aug 2015
Primary outcomePrimary: Parathyroid Hormone Level — 19; 20 pg/mL

Summary

This study recruits individuals with rheumatoid arthritis (RA) and low vitamin D concentrations. Subjects are dosed with vitamin D or placebo for one year. Primary outcome is change in bone turnover markers, additionally, bone mineral density and parameters of RA status are evaluated throughout the study.

Outcome Measures

OutcomeResultp-value
PRIMARY
Parathyroid Hormone Level
19; 20
SECONDARY
Bone Mineral Density
0.970; 1.151
SECONDARY
Short Form 36 Survey
39.1; 47.7

Eligibility Criteria

Inclusion Criteria

  • Rheumatology

Exclusion Criteria

  • Bisphosphonate therapy
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT00423358). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.

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