Genetic Study of Patients With Primary Ciliary Dyskinesia
2 other identifiers
observational
180
1 country
1
Brief Summary
OBJECTIVES: I. Characterize the clinical presentation of patients with primary ciliary dyskinesia. II. Identify the genetic mutations associated with this disease.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
February 1, 2000
CompletedFirst Submitted
Initial submission to the registry
May 2, 2000
CompletedFirst Posted
Study publicly available on registry
May 3, 2000
CompletedJune 24, 2005
December 1, 2003
May 2, 2000
June 23, 2005
Conditions
Keywords
Eligibility Criteria
Contact the study team to discuss eligibility requirements. They can help determine if this study is right for you.
Sponsors & Collaborators
Study Sites (1)
University of North Carolina School of Medicine
Chapel Hill, North Carolina, 27599-7070, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- STUDY CHAIR
Peadar G. Noone
University of North Carolina
Study Design
- Study Type
- observational
- Observational Model
- NATURAL HISTORY
- Sponsor Type
- NIH
Study Record Dates
First Submitted
May 2, 2000
First Posted
May 3, 2000
Study Start
February 1, 2000
Last Updated
June 24, 2005
Record last verified: 2003-12