Genetic Study of Patients With Primary Ciliary Dyskinesia

Completed

Conditions studied: Primary Ciliary Dyskinesia

In brief

OBJECTIVES: I. Characterize the clinical presentation of patients with primary ciliary dyskinesia. II. Identify the genetic mutations associated with this disease.

Key facts

Study ID

NCT00005650

Run by

National Center for Research Resources (NCRR)

People needed

180

Starts

2000-02-01

Last updated by the study team

2005-06-24

Who can join

Age: any. Sex: any. Healthy volunteers: not accepted.

Where it is running

• University of North Carolina School of Medicine — Chapel Hill, North Carolina, United States

Full record on ClinicalTrials.gov

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