NCT00005650

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

80
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
180

participants targeted

Target at P50-P75 for all trials

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

February 1, 2000

Completed
3 months until next milestone

First Submitted

Initial submission to the registry

May 2, 2000

Completed
1 day until next milestone

First Posted

Study publicly available on registry

May 3, 2000

Completed
Last Updated

June 24, 2005

Status Verified

December 1, 2003

First QC Date

May 2, 2000

Last Update Submit

June 23, 2005

Conditions

Keywords

cardiovascular and respiratory diseasesgenetic diseases and dysmorphic syndromesprimary ciliary dyskinesiarare disease

Eligibility Criteria

Age0 Years+
Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)
* Histologically or cytologically confirmed primary ciliary dyskinesia (PCD) * Family members of patients with PCD

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

Location

MeSH Terms

Conditions

Ciliary Motility DisordersRespiratory Tract DiseasesGenetic Diseases, InbornRare Diseases

Condition Hierarchy (Ancestors)

Otorhinolaryngologic DiseasesCiliopathiesAbnormalities, MultipleCongenital AbnormalitiesCongenital, Hereditary, and Neonatal Diseases and AbnormalitiesDisease AttributesPathologic ProcessesPathological Conditions, Signs and Symptoms

Study Officials

  • Peadar G. Noone

    University of North Carolina

    STUDY CHAIR

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

Locations