Little Rock, Arkansas 72202

  • Asthma

Purpose:

The primary objective of this study is to determine ex vivo the amount of fluticasone deposited onto a filter (delivered dose) interposed between the OptiChamber Diamond Valved Holding Chamber (VHC) mouthpiece and the subject's mouth during coordinated and uncoordinated actuation/inhalation maneuver.


Criteria:

Inclusion Criteria: - • Asthmatic children between the ages of 5 and 8 followed at Arkansas Children's Hospital. - The subjects must be available to complete the study. - The subject's parent(s) and/or the subject's legal guardian must provide written informed consent to participate in the study. - The subject must provide assent when older than 7 years old. - The subjects should have used a pMDI VHC previously and be able to use a VHC with mouthpiece. - The subjects should have been prescribed fluticasone or another inhaled corticosteroid delivered via a pMDI VHC combination. - Clinically stable asthma. - Cooperative, i.e., subject should be able to follow and understand instructions. - The subject must satisfy the study investigator about his/her fitness to participate in the study. Exclusion Criteria: - Clinically significant respiratory disease in the previous 4 weeks. - Participation in any other clinical trial in the previous 4 weeks. - Lack of cooperation, subject cannot follow and understand instructions.


NCT ID:

NCT01714063


Primary Contact:

Principal Investigator
Ariel Berlinski, MD
University of Arkansas


Backup Contact:

N/A


Location Contact:

Little Rock, Arkansas 72202
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: June 13, 2021

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