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Immunointervention With Calcitriol in New-Onset Type 1 Diabetes

Immunointervention With 1,25-dihydroxy-vitamin D3 in New-onset Type 1 Diabetes

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00960635
Enrollment
Unknown
Registered
2009-08-18
Start date
2001-06-30
Completion date
2008-08-31
Last updated
2009-08-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Type 1 Diabetes

Keywords

new-onset

Brief summary

This is a randomized, two-arm, placebo-controlled phase-2 trial to determine whether the daily intake of 1,25-dihydroxy-vitamin D3 \[1,25(OH)2D3\], improves beta cell function in patients with recently diagnosed type 1 diabetes. The treatment consists of the daily oral administration of 0.25 µg 1,25(OH)2D3 or placebo for 9 months and an equal follow-up time without supplementation. Fasting, peak and AUC C-peptide concentrations during a 2-hour mixed meal tolerance test are measured at the beginning of the study, as well as at the end of the treatment and the follow-up period in month 9 and 18. The null hypothesis is that there is no difference between 1,25(OH)2D3 treated subjects and the placebo group in the AUC C-peptide at month 18.

Interventions

DRUG1,25-dihydroxy-vitamin D3 (calcitriol)
DRUGplacebo

pill without agent

Sponsors

Institut fur Diabetesforschung, Munich, Germany
Lead SponsorOTHER

Study design

Primary purpose
PREVENTION

Eligibility

Sex/Gender
ALL
Age
18 Years to 39 Years

Inclusion criteria

* New onset Typ 1 diabetes (\< 6 weeks insulin therapy) * Age 18-39 years * GADA and/or IA-2A positive

Exclusion criteria

* Kidney disease * Pregnancy * Lactating

Countries

Germany

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026