PF-AtlasClinical Trials › NCT01812551

Treatment of Low Bone Density in Cystic Fibrosis.

Alendronate · Phase 3

Registry ID
NCT01812551
Phase
Phase 3
Status
Completed
Drug / intervention
Alendronate
Sponsor
Istituto Auxologico Italiano
Start
2002-10
Enrollment
171
Locations
11

About this trial

Cystic fibrosis (CF) -- an autosomal recessive genetic disease affecting about 60,000 individuals worldwide, including about 3,800 in Italy -- is often associated with low bone mineral mass. The current aggressive therapies have ensured a much longer survival of CF patients but this has led to a higher frequency of osteoporosis and bone fractures, a serious problem which not only affects quality of life, but also hinders further therapeutic measures. The aim of this study, conducted on a large group of children, adolescents and young adults with CF, has been the evaluation of bone mass changes after 1 year of a simple treatment with RDA-adjusted dietary calcium plus 25-OH vitamin D supplementation, and the feasibility and efficacy of alendronate treatment (for another year) in patients not responding to calcium + 25-OH vitamin D alone.

View NCT01812551 on ClinicalTrials.gov →

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Medical disclaimer. This page summarizes public trial data for NCT01812551 for information only. It is not medical advice, an endorsement, or an offer to enroll. Confirm details on ClinicalTrials.gov and with a qualified physician.