Clinical Trials & Research

Participation typically involves several study visits where you'll undergo Aridol testing along with standard spirometry. You'll also complete questionnaires about your symptoms and medical history. Most studies require 2-4 visits over several months. All testing is performed by trained respiratory technicians under physician supervision.

No, there is no cost to participate in our clinical trials. All study-related testing, medical care, and medications are provided at no charge. Participants also receive compensation for their time and reimbursement for travel expenses related to study visits.

Study visits typically last 2-3 hours, which includes time for consent review, medical history, spirometry testing, Aridol challenge test, and post-test monitoring. Your first visit may be longer as it includes screening procedures and detailed consent discussion. Follow-up visits are usually shorter.

Yes, participation in clinical research is completely voluntary. You can withdraw from a study at any time for any reason without penalty or loss of benefits to which you are entitled. Your decision will not affect your current or future medical care.

All clinical trials are reviewed and approved by an Institutional Review Board (IRB) to ensure participant safety. Testing is performed by certified respiratory technicians with emergency equipment and medications readily available. Participants are monitored closely during and after testing, and a physician is always available on-site.

Your privacy is protected under HIPAA regulations and study-specific confidentiality agreements. All study data is de-identified and stored securely. Only authorized study personnel have access to your personal information, and your identity will never be disclosed in any publications or presentations resulting from the research.