Tissue Bank for Pulmonary Diseases
NCT00546962 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 400
Last updated 2011-05-13
Summary
The aim of this research study is to collect and store the specimens that are left over after patients undergo tests ordered by their physicians. These specimens will be used at a later time by researchers in the Pulmonary Division to develop a better understanding of pulmonary diseases or for the development of new treatments. Typical research studies that will be conducted on the stored tissue, fluid, or bacteria from the patient sample involve obtaining bacterial cultures, measurement of inflammatory markers, and examination of the characteristics of the tissue. Other similar tests may be done in the future; however, these tests have not all been determined at this time. It is important to note that no genetic testing will be performed on any samples that are obtained as part of this protocol.
Conditions
Sponsors & Collaborators
- collaborator OTHER
- lead OTHER
Principal Investigators
-
Thomas Martin, MD · Boston Children's Hospital
Eligibility
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 1999-04-30
Countries
- United States
Study Locations
More Related Trials
-
Microbial Community Composition and Metabolism in Cystic Fibrosis
NCT00954018 ·Status: COMPLETED
-
Idiopathic Pulmonary Fibrosis: a Case-control Study
NCT00005295 ·Status: TERMINATED
-
Bronchial Inflammation of Small Airways in Patients With Cystic Fibrosis
NCT01479166 ·Status: COMPLETED
-
Comparing Chest Images From MRI to CT in Patients With Cystic Fibrosis (CF)
NCT01860872 ·Status: COMPLETED
-
Pinpointing the Factors Affecting Clinical Study Experiences of Pulmonary Fibrosis Patients
NCT05899556 ·Status: NOT_YET_RECRUITING
-
A National Registry on Chinese Patients With Cystic Fibrosis
NCT05289245 ·Status: RECRUITING
-
Molecular Phenotypes for Cystic Fibrosis Lung Disease
NCT01116414 ·Status: COMPLETED
-
Microbial Community Composition and Dynamics in Lungs of Cystic Fibrosis Sibling Pairs
NCT00590330 ·Status: COMPLETED
-
Development a Core Set for Adults With Cystic Fibrosis Based on the ICF
NCT06128499 ·Status: COMPLETED
-
Multicenter Study of Nontuberculous Mycobacteria in Cystic Fibrosis Patients
NCT00004296 ·Status: COMPLETED
-
Evaluating Sensations of Breathlessness in Patients With Cystic Fibrosis
NCT01799642 ·Status: COMPLETED
-
Microbiome Acquisition and Progression of Inflammation and Airway Disease in Infants and Children With Cystic Fibrosis
NCT01661491 ·Status: COMPLETED
-
Breath Condensate Study in Patients With Cystic Fibrosis.
NCT02056132 ·Status: COMPLETED
-
Pulmonary Vascular Disease in CF
NCT04549077 ·Status: ACTIVE_NOT_RECRUITING
-
Cystic Fibrosis (CF) Leukocyte Genes as Biomarkers for Novel Therapies
NCT00727285 ·Status: COMPLETED
-
Early Intervention in Cystic Fibrosis Exacerbation
NCT01104402 ·Status: COMPLETED ·Phase: NA
-
Pilot Observational Study to Determine Feasibility of a Standardized Treatment of Pulmonary Exacerb. in Patients With CF
NCT02109822 ·Status: COMPLETED
-
Analysis of Specimens From Individuals With Pulmonary Fibrosis
NCT00084305 ·Status: ACTIVE_NOT_RECRUITING
-
Bioavailability and Pharmacokinetics Study of FDL169 in Healthy Subjects and Subjects With Cystic Fibrosis
NCT02767297 ·Status: COMPLETED ·Phase: PHASE1/PHASE2
-
Cough Efficiency in Cystic Fibrosis
NCT01636219 ·Status: COMPLETED
-
Air Pollution and Children With Cystic Fibrosis
NCT03853629 ·Status: COMPLETED
-
Early Intervention in Pulmonary Exacerbation in Cystic Fibrosis
NCT00850551 ·Status: COMPLETED ·Phase: NA
-
Cystic Fibrosis Related Bone Disease: the Role of CFTR
NCT01549314 ·Status: COMPLETED
-
MENstrual Symptom Tracking to Understand and Assess (Women) Living With Cystic Fibrosis
NCT04620096 ·Status: COMPLETED
-
Pathogenesis of Primary Ciliary Dyskinesia (PCD) Lung Disease
NCT00807482 ·Status: RECRUITING