Impact on Reducing the Incidence of Low Serum Calcium by Providing Educational Materials on the Need to Take Daily Supplemental Calcium and Vitamin D to Patients With Paget's Disease Treated With Reclast®
Completed · Phase 4
Conditions studied: Paget's Disease of the Bone, Hypocalcemia
In brief
This study will evaluate the impact of investigator and patient education and educational materials to foster calcium and vitamin D supplementation to mitigate the potential for hypocalcemia post Reclast® administration in patients with Paget's disease of bone.
Key facts
- Study ID
- NCT00668200
- Run by
- Novartis Pharmaceuticals
- People needed
- 81
- Starts
- 2008-05-01
- Expected to finish
- 2012-11-01
- Last updated by the study team
- 2015-03-06
Who can join
Age: any. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Written informed consent
- As per currently approved Reclast® Package Insert:
You may not qualify if…
- As per currently approved Reclast® Package Insert:
Where it is running
- Novartis Investigative Site — Phoenix, Arizona, United States
- Novartis Investigative Site — Tucson, Arizona, United States
- Novartis Investigative Site — Gainesville, Georgia, United States
- Novartis Investigative Site — Detroit, Michigan, United States
- Novartis Investigative Site — Syracuse, New York, United States
- Novartis Investigative Site — Providence, Rhode Island, United States
- Novartis Investigative Site — Dallas, Texas, United States
- Novartis Investigative Site — Waco, Texas, United States
- Novartis Investigative Site — Madison, Wisconsin, United States
Full record on ClinicalTrials.gov
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