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Trial record 4 of 29 for:    Dermatophagoides pteronyssinus AND Dermatophagoides farinae

Screening Inhaled Allergen Challenge for Dermatophagoides Farinae (MiteScreen)

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ClinicalTrials.gov Identifier: NCT03049111
Recruitment Status : Recruiting
First Posted : February 9, 2017
Last Update Posted : March 19, 2019
Sponsor:
Collaborator:
National Heart, Lung, and Blood Institute (NHLBI)
Information provided by (Responsible Party):
University of North Carolina, Chapel Hill

Brief Summary:
This study is designed to identify Dermatophagoides farinae, or Der f, sensitive asthmatics who demonstrate a late phase asthmatic response after Der f inhalation. These subjects may be invited to participate in a planned future study investigating novel asthma treatments.

Condition or disease Intervention/treatment Phase
Asthma Biological: Der f Early Phase 1

  Show Detailed Description

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Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 100 participants
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Basic Science
Official Title: Screening Inhaled Allergen Challenge for Dermatophagoides Farinae
Actual Study Start Date : November 20, 2017
Estimated Primary Completion Date : March 2022
Estimated Study Completion Date : March 2022

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Asthma

Arm Intervention/treatment
Experimental: Inhaled Allergen Challenge
Der f sensitive, mild asthmatic subjects will undergo inhaled allergen challenge
Biological: Der f
Inhalation of Der f in mild asthmatics who are sensitive to Der f.
Other Names:
  • Dermatophagoides farinae
  • house dust mite




Primary Outcome Measures :
  1. Decline of FEV1 during the late phase response [ Time Frame: Pre-inhalation challenge and 3-10 hours after inhalation challenge ]
    Participants will undergo an inhaled allergen challenge to identify those with a measurable late phase response (LPR) to inhaled Dermatophagoides farinae allergen extract. Baseline FEV1 will be measured prior to administration of the allergen challenge. The presence of an LPR will be defined as a decline in FEV1 of ≥15% from baseline values 3-10 hours after the onset of the early phase response (which typically occurs within 30 minutes of allergen challenge).


Secondary Outcome Measures :
  1. Levels of IL-1β in induced sputum [ Time Frame: Baseline and 24 hours post- inhalation challenge ]
    Participants will undergo a hypertonic saline induced sputum procedure at baseline (within ~2 weeks of the allergen challenge), and again at 24 hours following inhaled allergen challenge. IL-1β concentrations in the sputum will be determined via ELISA. In addition to assessing changes in IL-1β levels, we will determine if IL-1β levels are predictive of key asthma outcomes following inhaled allergen challenge (see outcomes 3-7).

  2. Sputum granulocytes [ Time Frame: Baseline and 24 hours post- inhalation challenge ]
    Cellularity of sputum obtained at baseline and again at 24 hours following inhaled allergen challenge will be assessed.

  3. Mucins in sputum [ Time Frame: Baseline and 24 hours post- inhalation challenge ]
    Sputum mucins will be measured at baseline, and again at 24 hours following inhaled allergen challenge

  4. Maximum drop in FEV1 during the late phase response [ Time Frame: Pre-inhalation challenge and 3-10 hours after inhalation challenge ]
    FEV1 will be measured prior to administration of the inhaled allergen challenge. The maximum drop in FEV1 that occurs during the late phase (3-10 hours after challenge) will be determined.

  5. Airway hyper-responsiveness [ Time Frame: Baseline and 24 hours post- inhalation challenge ]
    Participants will undergo a methacholine challenge to assess airway hyper-responsiveness at baseline. Changes in methacholine reactivity from baseline to 24 hours after inhaled allergen challenge will be determined.

  6. Exhaled nitric oxide (eNO) levels [ Time Frame: Baseline and 24 hours post- inhalation challenge ]
    eNO levels will be measured at baseline, and 24 hours after inhaled allergen challenge.


Other Outcome Measures:
  1. Heart Rate Variability (HRV) [ Time Frame: Pre and immediately post challenge ]
    HRV with Spacelabs technology will be measured 24 hours pre and during inhalation challenge



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Ages Eligible for Study:   18 Years to 45 Years   (Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria

  1. Age range 18-45 years, inclusive
  2. FEV1 of at least 80% of predicted and forced expiratory volume in 1 second/forced vital capacity (FEV1/FVC) 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 intermittent or mild persistent asthma.
  3. Physician diagnosis of asthma
  4. Positive methacholine inhalation challenge as performed in the separate screening protocol within the prior 12 months (defined as provocative concentration of methacholine of 10 mg/ml or less producing a 20% fall in FEV1 (PC20 methacholine)
  5. Allergic sensitization to house dust mite (D. farinae) as confirmed by positive immediate skin prick test response
  6. Negative pregnancy test for females who are not s/p hysterectomy with oophorectomy or who have been amenorrheic for 12 months or more.
  7. Oxygen saturation of >94% and blood pressure within the following limits: (Systolic between 150-90 mmHg, Diastolic between 90-60 mmHg).

Exclusion Criteria

  1. Clinical contraindications:

    1. 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.
    2. Physician directed emergency treatment for an asthma exacerbation within the preceding 12 months.
    3. 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.
    4. 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).
    5. Viral upper respiratory tract infection within 4 weeks of challenge.
    6. Any acute infection requiring antibiotics within 6 weeks of exposure or fever of unknown origin within 6 weeks of challenge.
    7. Severe asthma
    8. 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.
    9. Cigarette smoking >1 pack per month
    10. 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.
    11. Allergy/sensitivity to study drugs or their formulations
    12. Known hypersensitivity to methacholine or to other parasympathomimetic agents
    13. History of intubation for asthma
    14. 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.
    15. Unwillingness to use reliable contraception if sexually active (IUD, birth control pills/patch, condoms).
  2. 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.
  3. Usage of the following medications:

    1. 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.
    2. 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.
    3. Use of daily theophylline within the past month.
    4. 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).
    5. Use of any immunosuppressant therapy within the preceding 12 months will be reviewed by the study physician.
    6. 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
    7. Use of beta blocking medications
    8. Antihistamines in the 5 days prior to allergen challenge
    9. Routine use of NSAIDs, including aspirin.
  4. Physical/laboratory indications:

    1. Abnormalities on lung auscultation
    2. Temperature >37.8 C
    3. Oxygen saturation of <94%
    4. Systolic BP>150 mmHg or <90 mmHg or diastolic BP>90 mmHg or <60 mmHg
  5. Inability or unwillingness of a participant to give written informed consent.

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03049111


Contacts
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Contact: Martha Almond, RCP 919-966-0759 martha_almond@med.unc.edu

Locations
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United States, North Carolina
UNC Center for Environmental Medicine, Asthma and Lung Biology Recruiting
Chapel Hill, North Carolina, United States, 27599-7310
Contact: Martha Almond    919-966-0759    martha_almond@med.unc.edu   
Principal Investigator: Michelle Hernandez, MD         
Sponsors and Collaborators
University of North Carolina, Chapel Hill
National Heart, Lung, and Blood Institute (NHLBI)
Investigators
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Principal Investigator: Michelle Hernandez, MD University of North Carolina

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Responsible Party: University of North Carolina, Chapel Hill
ClinicalTrials.gov Identifier: NCT03049111     History of Changes
Other Study ID Numbers: 16-2131
1R01HL135235-01A1 ( U.S. NIH Grant/Contract )
First Posted: February 9, 2017    Key Record Dates
Last Update Posted: March 19, 2019
Last Verified: March 2019
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: No

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Studies a U.S. FDA-regulated Drug Product: Yes
Studies a U.S. FDA-regulated Device Product: No

Keywords provided by University of North Carolina, Chapel Hill:
Der F (House Dust Mite)