Cystic Fibrosis Related Bone Disease: the Role of CFTR

NCT01549314 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 79

Last updated 2020-04-01

Study results available
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Summary

The purpose of this study is to determine whether ivacaftor, a recently FDA-approved CFTR potentiator, improves bone micro-architecture and strength in patients with cystic fibrosis with at least one G551D CFTR mutation.

Conditions

  • Cystic Fibrosis Related Bone Disease

Sponsors & Collaborators

Principal Investigators

  • Joel Finkelstein, MD · Massachusetts General Hospital

Eligibility

Min Age
6 Years
Max Age
75 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2012-04-30
Primary Completion
2018-05-31
Completion
2020-02-29

Countries

  • United States

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01549314 on ClinicalTrials.gov