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Transfer Impedance in Cystic Fibrosis (Ztr)
This study is currently recruiting participants.
Verified by Children's Hospital Boston, August 2008
Sponsored by: Children's Hospital Boston
Information provided by: Children's Hospital Boston
ClinicalTrials.gov Identifier: NCT00743158
  Purpose

This study aims to determine whether respiratory system transfer impedance (Ztr) may fill an important clinical function by providing a reproducible, valid, and sensitive measure of airway obstruction in people with CF.


Condition
Cystic Fibrosis

Genetics Home Reference related topics: cystic fibrosis
MedlinePlus related topics: Cystic Fibrosis
U.S. FDA Resources
Study Type: Observational
Study Design: Case-Only, Prospective
Official Title: Transfer Impedance in Cystic Fibrosis (Ztr)

Further study details as provided by Children's Hospital Boston:

Biospecimen Retention:   None Retained

Biospecimen Description:

Estimated Enrollment: 40
Study Start Date: August 2008
  Eligibility

Ages Eligible for Study:   2 Years to 25 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Sampling Method:   Probability Sample
Study Population

Cystic Fibrosis Patients

Criteria

Inclusion Criteria:

  • Between the ages of 2 to 25 Confirmed diagnosis of Cystic Fibrosis

Exclusion Criteria:

  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00743158

Locations
United States, Massachusetts
Childrens Hospital, Boston Recruiting
Boston, Massachusetts, United States, 02115
Contact: Lamia Momen, BA     617-355-6665     lamia.momen@childrens.harvard.edu    
Principal Investigator: Thomas R Martin, MD            
Sponsors and Collaborators
Children's Hospital Boston
  More Information

Responsible Party: Childrens Hospital, Boston ( Thomas Martin, MD )
Study ID Numbers: X08-01-0060
Study First Received: August 27, 2008
Last Updated: August 27, 2008
ClinicalTrials.gov Identifier: NCT00743158  
Health Authority: United States: Institutional Review Board

Keywords provided by Children's Hospital Boston:
ztr
transfer impedance
cystic fibrosis
pulmonary function test
pft

Study placed in the following topic categories:
Digestive System Diseases
Genetic Diseases, Inborn
Respiratory Tract Diseases
Cystic Fibrosis
Fibrosis
Lung Diseases
Infant, Newborn, Diseases
Pancreatic Diseases
Cystic fibrosis

Additional relevant MeSH terms:
Pathologic Processes

ClinicalTrials.gov processed this record on January 16, 2009