Assessing Mucociliary Clearance and Airway Liquid Volume in the CF Airway
NCT00248755 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 14
Last updated 2017-07-25
Summary
The objective of this study is to determine the effect of airway surface liquid (ASL) volume on mucociliary clearance in cystic fibrosis (CF). A two-isotope nuclear medicine technique will be utilized. This pilot trial will include the imaging of n=7 CF subjects and n=7 healthy subjects. The trial will include one study visit per subject that will take approximately 3 hours. Hypothesis: The simultaneous imaging of both a "floating" and a "penetrating" radioisotope tag will allow the relative effect of airway surface liquid volume on mucociliary clearance to be determined when evaluated in CF and normal subjects.
Conditions
Interventions
- PROCEDURE
-
mucociliary clearance scan
Sponsors & Collaborators
-
Cystic Fibrosis Foundation
collaborator OTHER -
University of Pittsburgh
lead OTHER
Principal Investigators
-
Timothy E Corcoran, Ph.D. · University of Pittsburgh
Study Design
- Allocation
- NON_RANDOMIZED
- Purpose
- DIAGNOSTIC
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2005-11-30
- Completion
- 2006-08-31
Countries
- United States
Study Locations
More Related Trials
-
Non-contrast Lung Perfusion Mapping Applied for New Insights in Cystic Fibrosis
NCT04467957 ·Status: ACTIVE_NOT_RECRUITING ·Phase: PHASE4
-
Airway Clearance Therapy on Hyperpolarized 129Xenon and MRI
NCT03593434 ·Status: COMPLETED
-
Airway Secretion Clearance in Cystic Fibrosis
NCT00839644 ·Status: TERMINATED ·Phase: NA
-
Regional Phenotyping of CF and Non-CF Bronchiectasis
NCT04793867 ·Status: RECRUITING
-
Early Assessment of Respiratory Function, Inflammation and Bronchial Reshuffle Among Newborns Screened for Cystic Fibrosis
NCT02883816 ·Status: COMPLETED ·Phase: NA
-
Using Rheological Methods to Characterize Cystic Fibrosis (CF) Sputum and the Effects of Mucoactive Agents
NCT00758771 ·Status: COMPLETED
-
Effects of Kalydeco on Upper Airway and Paranasal Sinus Inflammation Measured by Nasal Lavage and on Symptoms
NCT02311140 ·Status: COMPLETED
-
Tissue Collection From People With Cystic Fibrosis
NCT00015756 ·Status: COMPLETED
-
Sputum Purulence as a Predictor of Cystic Fibrosis Exacerbations: a Prospective Cohort Trial.
NCT02309229 ·Status: COMPLETED
-
Feasibility of Home-based Exercise Program for Adults With Cystic Fibrosis
NCT05239611 ·Status: COMPLETED ·Phase: PHASE2
-
Researching the Effects of Airway Clearance Therapies in Cystic Fibrosis
NCT03078127 ·Status: COMPLETED ·Phase: NA
-
Comparison of Airway Clearance Efficacy of Two High Frequency Chest Wall Oscillation (HFCWO) Devices in Cystic Fibrosis
NCT00308958 ·Status: COMPLETED ·Phase: NA
-
Evaluation of Sit-to-stand Test in Patients With Cystic Fibrosis and Matched Controls.
NCT03524859 ·Status: COMPLETED
-
Comparing Chest Images From MRI to CT in Patients With Cystic Fibrosis (CF)
NCT01860872 ·Status: COMPLETED
-
Evaluating High Flow Humidification Therapy in Patients With Cystic Fibrosis
NCT02129803 ·Status: COMPLETED ·Phase: NA
-
Timing of Hypertonic Saline Inhalation Relative to Airways Clearance in Cystic Fibrosis
NCT01753869 ·Status: TERMINATED ·Phase: NA
-
Study to Enable New Diagnostics for Pulmonary Microbes in People With CF
NCT07312734 ·Status: NOT_YET_RECRUITING
-
Monitoring Response to Orkambi in Cystic Fibrosis Lung Disease by Inhaled Xenon MRI
NCT02848560 ·Status: ACTIVE_NOT_RECRUITING
-
Tracking CF Lung Disease Through the Early Years: Utility of the LCI
NCT03138772 ·Status: COMPLETED
-
Evaluation of Lung T1-MRI in Pediatric Cystic Fibrosis Patients
NCT04994301 ·Status: COMPLETED
-
Utility of Induced Sputum Using Hypertonic Saline to Evaluate Infection and Inflammation in Cystic Fibrosis
NCT00721071 ·Status: COMPLETED ·Phase: PHASE2
-
Using MRI to Observe Lung Changes in Infants With CF Compared to Infants Without CF
NCT01832519 ·Status: COMPLETED
-
PATIENCE Trial: Prospective Algorithm for Treatment of NTM in Cystic Fibrosis
NCT02419989 ·Status: ENROLLING_BY_INVITATION
-
Comparison Between RTX (Biphasic Cuirass Ventilator) and Physiotherapy in Cystic Fibrosis Patients
NCT00908505 ·Status: UNKNOWN ·Phase: NA
-
Controlled Ventilation CT in CF Infants
NCT01200888 ·Status: TERMINATED