Status:
TERMINATED
Identification of Allergic Asthmatics Reactive to Felis Catus (Cat Hair) Allergen Inhalation
Lead Sponsor:
University of North Carolina, Chapel Hill
Collaborating Sponsors:
National Heart, Lung, and Blood Institute (NHLBI)
Conditions:
Asthma Atopic
Eligibility:
All Genders
18-45 years
Phase:
EARLY_PHASE1
Brief Summary
This study is designed to identify Felis Catus, or cat hair, sensitive asthmatics who demonstrate a late phase asthmatic response after cat hair inhalation. These subjects may be invited to participat...
Detailed Description
Asthma is an increasingly common chronic illness among children and adults, and allergen exposure is among the most common triggers for asthma exacerbations. Exacerbations of allergic asthma are chara...
Eligibility Criteria
Inclusion
- Age range 18-45 years, inclusive
- FEV1 of at least 80% of predicted and FEV1/FVC (Forced Vital Capacity) ratio of at least 0.7 (without use of bronchodilator medications for 8 hours or long acting beta agonists for 24 hours), consistent with lung function of persons with no more than mild episodic or mild persistent asthma.
- Physician diagnosis of asthma
- Allergic sensitization to felis catus (cat hair) as confirmed by positive immediate skin prick test response
- Negative pregnancy test for females who are not s/p hysterectomy or who have been amenorrheic for 12 months or more.
- Oxygen saturation of \>94% and blood pressure within the following limits: (Systolic between 150-90 mmHg, Diastolic between 90-60 mmHg).
Exclusion
- Clinical contraindications:
- Any chronic medical condition considered by the PI as a contraindication to participation in the study including significant cardiovascular disease, diabetes, chronic renal disease, chronic thyroid disease, history of chronic infections or immunodeficiency.
- Physician directed emergency treatment for an asthma exacerbation within the preceding 12 months.
- Exacerbation of asthma more than 2x/week which could 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 requirements 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 4 weeks of challenge.
- Any acute infection requiring antibiotics within 6 weeks of exposure or fever of unknown origin within 6 weeks of challenge.
- Severe asthma
- Mental illness or history of drug or alcohol abuse that, in the opinion of the investigator, would interfere with the participant's ability to comply with study requirements.
- 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.
- Allergy/sensitivity to study drugs or their formulations
- Known hypersensitivity to methacholine or to other parasympathomimetic agents
- History of intubation for asthma
- Unwillingness to avoid coffee, tea, cola drinks, chocolate, or other foods containing caffeine after midnight on the days that methacholine challenge testing is to be performed.
- Unwillingness to use reliable contraception if sexually active (IUD, birth control pills/patch, condoms).
- Pregnancy or nursing a baby. Female volunteers will be asked to use effective birth control (stable regimen of hormonal contraceptive use for at least 3 months, intrauterine device placement, tubal ligation or endometrial ablation for at least 3 months through at least one week after study completion) and will provide a urine sample to test for pregnancy on study days. If the test is positive or the subject has reason to believe she may be pregnant, she will be dismissed from the study. Women who have been amenorrheic for 12 months may participate. Male volunteers will be asked to use condoms for the duration of the study through at least one week after study completion.
- Usage of the following medications:
- 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.
- Subjects who are prescribed daily inhaled corticosteroids, cromolyn, or leukotriene inhibitors (Montelukast or Zafirlukast) will be required to discontinue these medications at least 2 weeks prior to their screening visit.
- Use of daily theophylline within the past month.
- 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).
- Use of any immunosuppressant therapy within the preceding 12 months will be reviewed by the study physician.
- Receipt of Live Attenuated Influenza Vaccine (LAIV), also known as FluMist®, or any other live viral vaccine within the prior 30 days, or any vaccine for at least 5 days
- Use of beta blocking medications
- Antihistamines in the 5 days prior to allergen challenge
- Routine use of NSAIDs, including aspirin.
- Physical/laboratory indications:
- Abnormalities on lung auscultation
- Temperature \>37.8°C
- Oxygen saturation of \<94%
- Systolic BP\>150 mmHg or \<90 mmHg or diastolic BP\>90 mmHg or \<60 mmHg
- Inability or unwillingness of a participant to give written informed consent
Key Trial Info
Start Date :
April 16 2019
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
November 11 2019
Estimated Enrollment :
1 Patients enrolled
Trial Details
Trial ID
NCT03780387
Start Date
April 16 2019
End Date
November 11 2019
Last Update
October 18 2022
Active Locations (1)
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1
Katie Mills
Chapel Hill, North Carolina, United States, 27599