- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01661374
The Effect of Humidification on Mucus Rheology
December 9, 2014 updated by: Virginia Commonwealth University
In this study the investigators will collect mucus from mechanical ventilated patients and patients with COPD to study the effect of temperature and humidity, on the biophysical properties of the airway mucus.
It is hypothesised that changes in inspired gas temperature and humidity (over time) may affect the biophysical properties of the airway mucus and reduce the airway's ability to clear mucus, resulting in deleterious clinical affects.
Study Overview
Status
Completed
Conditions
Detailed Description
Expectorated sputum samples are collected and used to measure the biophysical properties of mucus secretions.
The samples are later exposed to different temperatures and humidity levels during bench experiments.
Study Type
Observational
Enrollment (Actual)
18
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Virginia
-
Richmond, Virginia, United States, 23284
- Virginia Commonwealth University
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
40 years to 90 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Primary Care Clinic,ICU, Pulmonary Clinic
Description
Mechanically Ventilated Patients
Inclusion Criteria:
Any Subject Mechanically Ventilated and producing sputum.
Exclusion
- None
COPD Group
Inclusion Criteria:
- 40 to 90 years of age suffering from COPD
- History of mucus production
Exclusion Criteria:
- None
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
|---|
|
Mechanically Ventilated
|
|
Chronic obstructive pulmonary disease (COPD).
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Sputum Collection
Time Frame: 10 minutes
|
Sputum is collected during pulmonary function test (PFT) to later measure the biophysical properties of sputum.
|
10 minutes
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Principal Investigator: Bruce K Rubin, MEngr, MD, MBA, FRCPC, Virginia Commonwealth University School of Medicine
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
July 1, 2012
Primary Completion (Actual)
April 1, 2014
Study Completion (Actual)
April 1, 2014
Study Registration Dates
First Submitted
August 6, 2012
First Submitted That Met QC Criteria
August 8, 2012
First Posted (Estimate)
August 9, 2012
Study Record Updates
Last Update Posted (Estimate)
December 10, 2014
Last Update Submitted That Met QC Criteria
December 9, 2014
Last Verified
December 1, 2014
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- HM14433
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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