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Diagnosis and Treatment of Patients With Cystic Fibrosis

National Institutes of Health (NIH) logo

National Institutes of Health (NIH)

Status

Enrolling

Conditions

Diabetes
Pancreatic Insufficiency (Exocrine and Endocrine)
Cystic Fibrosis
Liver Disease or Abnormalities

Study type

Observational

Funder types

NIH

Identifiers

NCT00001223
87-DK-0029
870029

Details and patient eligibility

About

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.

Full 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.

Enrollment

9,999 estimated patients

Sex

All

Ages

4 to 120 years old

Volunteers

Accepts Healthy Volunteers

Inclusion and exclusion criteria

  • 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.

Trial design

9,999 participants in 2 patient groups

CF Patients
Description:
cystic fibrosis patients
CF Relatives
Description:
relatives of cystic fibrosis patients

Trial contacts and locations

1

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Central trial contact

Milica S Chernick, M.D.

Data sourced from clinicaltrials.gov

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