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Safety Study of 20,000 EU of Clinical Center Reference Endotoxin in Allergic Adults With and Without Mild Asthma

Primary Purpose

Mild Allergic Rhinitis, Mild Allergic Rhinitis With Mild Asthma

Status
Terminated
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
Clinical Center Reference Endotoxin
Sponsored by
University of North Carolina, Chapel Hill
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional basic science trial for Mild Allergic Rhinitis focused on measuring mild asthma, mild allergies

Eligibility Criteria

18 Years - 50 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Mild allergic rhinitis
  • Mild allergic asthma
  • Normal lung function
  • No other chronic illness

Exclusion Criteria:

  • Use of inhaled or oral steroids
  • Emergency treatment of asthma in last year
  • Inhaled tobacco use

Sites / Locations

  • UNC Center for Environmental Medicine, Asthma and Lung Biology

Outcomes

Primary Outcome Measures

Increased sputum neutrophils with no adverse events

Secondary Outcome Measures

Full Information

First Posted
February 28, 2008
Last Updated
October 5, 2012
Sponsor
University of North Carolina, Chapel Hill
Collaborators
National Institutes of Health (NIH)
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1. Study Identification

Unique Protocol Identification Number
NCT00630461
Brief Title
Safety Study of 20,000 EU of Clinical Center Reference Endotoxin in Allergic Adults With and Without Mild Asthma
Official Title
Safety Study of 20,000 EU of Clinical Center Reference Endotoxin in Allergic Adults With and Without Mild Asthma
Study Type
Interventional

2. Study Status

Record Verification Date
October 2012
Overall Recruitment Status
Terminated
Why Stopped
Data collected under different protocol; funding exhuasted
Study Start Date
May 2008 (undefined)
Primary Completion Date
May 2012 (Actual)
Study Completion Date
May 2012 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of North Carolina, Chapel Hill
Collaborators
National Institutes of Health (NIH)

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Endotoxin is a component of outdoor air pollution, an air contaminant found in a number of different workplaces, and is even found in homes. The endotoxin used for this study is obtained from the National Institutes of Health, and is called "Clinical Center Reference Endotoxin", or CCRE. The purpose of this Phase 1 research study is to identify a dose of inhaled endotoxin that is safe (does not cause prolonged cough, shortness of breath or other problems), but causes changes in your sputum cell samples that the scientists can measure. Phase 1 research studies like this one are not intended to be a treatment, but are a scientific investigation. Eventually, with these types of studies we will be able to examine why some people are more sensitive to endotoxin. Scientists at other universities have found that while most people do not have a considerable lung response to endotoxin at doses as high as 60,000 EU (endotoxin units), a few respond to as little as a total dose of 4500 EU. Our study is designed to identify if using a dose of 20,000 EU causes changes in the lung cells but does not cause symptoms in our study subjects. In our previous studies in our lab, using an endotoxin from another source, we have used higher doses (15,000 EUs) in subjects with asthma with no major problems, and we have used 10,000 EUs of CCRE in subjects with allergies and asthma without problems. We have used 20,000 EUs of CCRE in healthy individuals with no major problems.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Mild Allergic Rhinitis, Mild Allergic Rhinitis With Mild Asthma
Keywords
mild asthma, mild allergies

7. Study Design

Primary Purpose
Basic Science
Study Phase
Phase 1
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
4 (Actual)

8. Arms, Groups, and Interventions

Intervention Type
Biological
Intervention Name(s)
Clinical Center Reference Endotoxin
Intervention Description
single inhalation challenge
Primary Outcome Measure Information:
Title
Increased sputum neutrophils with no adverse events
Time Frame
6 hours post challenge

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Mild allergic rhinitis Mild allergic asthma Normal lung function No other chronic illness Exclusion Criteria: Use of inhaled or oral steroids Emergency treatment of asthma in last year Inhaled tobacco use
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
David b Peden, MD, MS
Organizational Affiliation
University of North Carolina
Official's Role
Principal Investigator
Facility Information:
Facility Name
UNC Center for Environmental Medicine, Asthma and Lung Biology
City
Chapel Hill
State/Province
North Carolina
ZIP/Postal Code
27599
Country
United States

12. IPD Sharing Statement

Learn more about this trial

Safety Study of 20,000 EU of Clinical Center Reference Endotoxin in Allergic Adults With and Without Mild Asthma

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