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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT00001223
Other study ID # 870029
Secondary ID 87-DK-0029
Status Recruiting
Phase
First received
Last updated
Start date January 1, 1988

Study information

Verified date February 9, 2024
Source National Institutes of Health Clinical Center (CC)
Contact Milica S Chernick, M.D.
Phone (301) 496-3434
Email milicac@bdg10.niddk.nih.gov
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This is an omnibus protocol for studying patients with cystic fibrosis. The main purpose of the study is to obtain samples and data collected during standard clinical care for future research to expand knowledge of the natural history, clinical manifestations (phenotypes) and the genetic variants (genotypes) of cystic fibrosis....


Description:

This is an omnibus protocol for studying patients with cystic fibrosis. The main purpose of the study is to obtain samples and data collected during standard clinical care for future research to expand knowledge of the natural history, clinical manifestations (phenotypes) and the genetic variants (genotypes) of cystic fibrosis.


Recruitment information / eligibility

Status Recruiting
Enrollment 9999
Est. completion date
Est. primary completion date
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 4 Years to 120 Years
Eligibility - INCLUSION CRITERIA - Patients with known or suspected CF and family members of patients with CF. - >=4 years of age EXCLUSION CRITERIA -Concomitant medical, psychiatric or other problems which might complicate interpretation of studies of CF, or for which we are unable to provide adequate care.

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
United States National Institutes of Health Clinical Center Bethesda Maryland

Sponsors (1)

Lead Sponsor Collaborator
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary To develop a database and collection of samples obtained from patients with CF during their clinical care to allow for future research To develop a collection of samples and a database from patients with cystic fibrosis to be used in future research. end of study
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