RecruitingNot ApplicableNCT07288827

Examining Bronchial Hyperresponsiveness in Primary Ciliary Dyskinesia

A Multi-center Study Examining Bronchial Hyperresponsiveness in Primary Ciliary Dyskinesia


Sponsor

Indiana University

Enrollment

40 participants

Start Date

May 4, 2023

Study Type

INTERVENTIONAL

Conditions

Summary

The purpose of this study is to look at children with PCD and see if they have another condition called "bronchial hyperresponsiveness".


Eligibility

Min Age: 6 Years

Inclusion Criteria4

  • Confirmed diagnosis of PCD per standard diagnostic criteria4 and positive genetics
  • Age greater than or equal to 6 years (no upper age limit)
  • Any gender or race
  • Able to perform pulmonary function testing (historical documentation of reversibility will be accepted)

Exclusion Criteria2

  • history of current pneumothorax
  • inability to perform pulmonary function testing

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Interventions

PROCEDURELung Function Testing

will include baseline spirometry (pre- and post- max bronchodilator). All testing will be done according to American Thoracic Society/European Respiratory Society guidelines. Participants will be asked to refrain from taking any asthma medications, including inhaled corticosteroids, short- and long-acting bronchodilators, leukotriene receptor antagonists, and long-acting muscarinic antagonists, for 24 hours prior to any spirometry. This activity will take place at a clinical research center at the respective participating institution.

PROCEDUREPhlebotomy

will be obtained at visit 2. Up to ten (10) ml of blood will be collected for measurement of serum biomarkers of atopy, based on whether participants prefer to receive an allergy skin prick test or have antigen-specific IgE levels tested. In the event a subject refuses phlebotomy, historical results up to one year old may be used in lieu of prospective results. Any remaining blood samples will be banked either for use in future studies or in the event that additional serum biomarkers are added to this study.

PROCEDUREAllergy skin prick testing

may be completed at visit 2. Subjects will be instructed to withhold first-generation antihistamines for 3 days and second-generation antihistamines for 7 days prior to the test. If patients prefer to have serum antigen-specific IgE levels run with the required serum biomarkers of atopy, then skin prick testing will be omitted.

PROCEDUREMethacholine Challenge

If the subject does not demonstrate a bronchodilator response in FEV1 of 10% or greater, and does not have a historical MCT on file, MCT will be performed. Following inhalation of saline, methacholine (MCh) will be inhaled in quadrupling concentrations starting with 0.0625 mg/ml and continuing until the MCh concentration required for FEV1 to decrease by 20% from baseline (PD20) is achieved or a maximum MCh concentration of 16 mg/ml is inhaled.


Locations(1)

Riley Hospital for Children

Indianapolis, Indiana, United States

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