Diagnosis and Treatment of Patients With Cystic Fibrosis

Sponsor
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) (NIH)
Overall Status
Recruiting
CT.gov ID
NCT00001223
Collaborator
(none)
9,999
1

Study Details

Study Description

Brief 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.

Detailed 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.

Study Design

Study Type:
Observational
Anticipated Enrollment :
9999 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Diagnosis and Treatment of Patients With Cystic Fibrosis
Actual Study Start Date :
Jan 1, 1988

Arms and Interventions

Arm Intervention/Treatment
CF Patients

cystic fibrosis patients

CF Relatives

relatives of cystic fibrosis patients

Outcome Measures

Primary Outcome Measures

  1. To develop a database and collection of samples obtained from patients with CF during their clinical care to allow for future research [end of study]

    To develop a collection of samples and a database from patients with cystic fibrosis to be used in future research.

Eligibility Criteria

Criteria

Ages Eligible for Study:
4 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
  • 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.

Contacts and Locations

Locations

Site City State Country Postal Code
1 National Institutes of Health Clinical Center, 9000 Rockville Pike Bethesda Maryland United States 20892

Sponsors and Collaborators

  • National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)

Investigators

  • Principal Investigator: Milica S Chernick, M.D., National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)

Study Documents (Full-Text)

None provided.

More Information

Additional Information:

Publications

None provided.
Responsible Party:
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
ClinicalTrials.gov Identifier:
NCT00001223
Other Study ID Numbers:
  • 870029
  • 87-DK-0029
First Posted:
Nov 4, 1999
Last Update Posted:
Aug 25, 2022
Last Verified:
Jan 13, 2022
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Additional relevant MeSH terms:

Study Results

No Results Posted as of Aug 25, 2022