| City: |
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Chapel Hill |
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State:
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NC |
| Zip Code: |
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27599 |
| Conditions: |
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Asthma - Hypersensitivity |
| Purpose: |
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This will be a single center, open label study comparing baseline characteristics of
recovered sputum cells (collected on screening day) to those of cells recovered 6 hours
after inhalational challenge with 20,000 EU Clinical Center Reference Endotoxin (CCRE, a
component of air pollution)) within each group as well as cross group comparisons between
individuals with allergic asthma (AA's)and normal volunteers (NV's). The primary objective
of this study is to test the hypothesis that persons with allergic asthma will have an
increased neutrophil response to challenge with 20,000 EU CCRE compared to normal
volunteers. Secondary objectives include post CCRE comparison between AA's and NV's with
regard to changes in airway cells and blood as well as changes in mucociliary clearance
(MCC) in response to inhalation of 20,000 EU CCRE.
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| Study summary: |
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This will be a single center, open label study of allergic asthmatic and normal volunteers.
The protocol will compare baseline characteristics of recovered sputum cells (collected on
screening day) to those of cells recovered 6 hours after inhalational challenge with CCRE
within each group as well as cross group comparisons between AA's and NV's. The following
information indicates procedures to be performed at each visit as well as the anticipated
duration of visits. Subsequent to this description are details regarding specific study
procedures.
Visit 1: Baseline Visit (5 hours)
1. Consent will be obtained, review of subject's medical history, current medications and
inclusion/exclusion criteria.
2. Vital sign measurements (temperature, pulse, respiratory rate, blood pressure), oxygen
saturation, and symptom scoring
3. Urine pregnancy test for women of child bearing potential
4. Spirometry
5. Venipuncture for CBC with differential and baseline blood analyses
6. Physical exam of the ears, nose, throat and chest
7. Collection of exhaled breath for measurement of nitric oxide level
8. Xenon equilibrium gas scan and MCC
9. MCC scan
10. Sputum induction
11. After completion of the sputum induction, subjects will have brief MCC scan (< 10
minutes)
Visit 2: 24 hours post baseline subjects will return for the following 1 hour visit:
1. Review any change in medical status over prior 24 hours, vital signs, O2 saturation and
symptom score
2. Follow up MCC scan
Visit 3: 24-48 hours prior to challenge visit at least 2 days after the baseline visit (½
hour)
1. Review change in medical status since last visit; vital signs, oxygen saturation, &
symptom score
2. Urine pregnancy test
3. Spirometry
Visit 4: Endotoxin (CCRE) challenge day (8.5 to 9 hours)
1. Review any change in medical status since last visit
2. Vital signs, oxygen saturation, and symptom score
3. Spirometry
4. Physical exam of the ears, nose, throat and chest
5. If above measures are acceptable, CCRE challenge will be performed
6. Post-challenge monitoring including spirometry, vital signs, oxygen saturation, and
symptom score at the following intervals post challenge: 30 and 60 minutes and then
hourly for 5 additional hours.
7. Post challenge venipuncture (blood draw) for CBC with differential and post CCRE blood
analyses
8. Collection of exhaled breath for measurement of nitric oxide level.
9. Four hours post challenge, subject will have MCC evaluated
10. After MCC is assessed, sputum induction will be performed.
11. After completion of the sputum induction, subjects will have brief MCC scan (< 10
minutes)
12. Discharge home or, alternatively, to GCRC for overnight observation per study MD.
Visit 5: 24 hours post challenge visit (1 hour)
1. Subject returns to the CEMALB, vital signs, oxygen saturation, and symptom score
2. Collection of exhaled breath for measurement of nitric oxide level.
3. Spirometry
4. Follow-up MCC scan
5. Each volunteer will be given a symptom scoring sheet for each day up to 96 hours (4
days) after challenge (see accompanying symptom scoring sheet in Appendix 3).
Post Challenge Observations/Reporting (5 minutes)
1. Subjects will be contacted for phone call follow-up 48-96 hours after challenge (see
script Appendix 4 of accompanying protocol)
Study discontinuation visit within 10 days of the challenge dose: (15 minutes)
1. Vital signs, O2 saturation, symptom score, spirometry
2. If any findings are abnormal, medical evaluation as directed by the study physician
will be undertaken Appendix 1 of the accompanying protocol provides a summary table
regarding procedures performed at each subject study visit |
| Criteria: |
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Inclusion Criteria for healthy controls:
- Normal lung function, defined as (Knudson 1976/1984 predicted set):
FVC of > 80 % of that predicted for gender, ethnicity, age and height FEV1 of > 80 % of
that predicted for gender, ethnicity, age and height FEV1/FVC ratio of > .75
- Oxygen saturation of > 94 % and normal blood pressure (Systolic between 150 - 90,
Diastolic between 90-60 mm Hg)
- Symptom Score no greater than 6 (out of a possible 24) for total symptom score with a
value no greater than 2 for any one score.
- Negative methacholine inhalation challenge as performed in the screening protocol.
(Less than a 20% decrease in FEV1 at a maximum methacholine concentration of 10
mg/ml)
--Negative pregnancy test for females
- Negative allergy skin test (AST)
Inclusion criteria for allergic asthmatics also include:
- History of episodic wheezing, chest tightness, or shortness of breath after age of 6
years consistent with asthma, or physician diagnosed asthma after age of 6 years.
- Positive methacholine test.
- FEV1 of at least 80% of predicted and FEV1/FVC ratio of at least .70 (without use of
bronchodilating medications for 12 hours)
- Allergic sensitization to at least one of the following allergen preparations: (House
Dust Mite f, House dust mite p, Cockroach, Tree mix, Grass Mix, Weed Mix, Mold Mix 1,
Mold Mix 2, Rat, Mouse, Guinea Pig, Rabbit, Cat or Dog) confirmed by positive AST.
- Negative allergy skin test as performed in the screening protocol.
Exclusion Criteria:
- Any chronic medical condition considered by the PI as a contraindication to the
exposure study including significant cardiovascular disease, diabetes requiring
medication, chronic renal disease, or chronic thyroid disease.
- Physician directed emergency treatment for an asthma exacerbation within the
preceding 12 months.
- Use of systemic steroid therapy within the preceding 12 months for an asthma
exacerbation. All use of systemic steroids in the last year will be reviewed by a
study physician.
- Use of inhaled steroids, cromolyn or leukotriene inhibitors (montelukast or
zafirlukast) except for use of cromolyn exclusively prior to exercise.
- Use of daily theophylline within the past month.
- Use of tricyclics and MAO inhibitors
- Pregnancy or nursing a baby.
- Cigarette smoking > 1 pack per month.
- Nighttime symptoms of cough or wheeze greater than 1x/week at baseline (not during a
clearly recognized viral induced asthma exacerbation) which would be characteristic
of a person of moderate or severe persistent asthma as outlined in the current NHLBI
guidelines for diagnosis and management of asthma.
- Exacerbation of asthma more than 2x/week which would be characteristic of a person of
moderate or severe persistent asthma as outlined in the current NHLBI guidelines for
diagnosis and management of asthma.
- Daily requirement for albuterol due to asthma symptoms (cough, wheeze, chest
tightness) which would be characteristic of a person of moderate or severe persistent
asthma as outlined in the current NHLBI guidelines for diagnosis and management of
asthma. (Not to include prophylactic use of albuterol prior to exercise).
- Viral upper respiratory tract infection within 2 weeks of challenge.
- Any acute infection requiring antibiotics within 2 weeks of challenge
- Receipt of LAIV (Live Attenuated Influenza Vaccine), also know as FluMist®, within
the prior 14 days |
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| Study is available at: |
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UNC Center for Environmental Medicine, Asthma and Lung Biology
Chapel Hill, NC 27599
United States
Primary Contact:
Peg Herbst, RN, MSN
Email: margaret_herbst@med.unc.edu
Phone: 919-966-2879 |
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If you are interested in this clinical trial please use the contact information above. If you would like to get additional information about this clinical trial please visit ClinicalTrials.gov.
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| Data Source: |
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ClinicalTrials.gov |
| Date Processed: |
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March 23, 2011 |
Modifications to
this listing: |
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above to view all information about this clinical trial. |
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