drugset / Trial / NCT00114803
Nasal Calcitonin in the Treatment of Bone Mineral Loss in Children and Adolescents With Inflammatory Bowel Disease
Completed
66 enrolled
Boston Children's Hospital
Crohn's and Colitis Foundation · collabNational Institutes of Health (NIH) · collab
RandomizedParallel-groupDouble-blind
Summary
The hypothesis underlying this study is that nasally administered calcitonin will stabilize or improve bone mineral density in young patients with ulcerative colitis or Crohn's disease. Patients who participate will receive either calcitonin or placebo and will have their bone mineral density measured at the start, at nine months, and at 18 months of study. Participants will also receive age appropriate doses of vitamin D and calcium supplements. Other serological measures of vitamin D status will be obtained every 3 months during the study.
Timeline
- Start
- 2004-01
- Primary completion
- —
- Completion
- 2006-10
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Calcitonin | Protein / enzyme biologic | — | Intranasal |