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Advanced Diagnostics in Patients with Respiratory Symptoms

Overview

About this study

The purpose of this study is to determine the best Impulse oscillometry( IOS)  device to improve diagnostic phemotyping and early detection of changes in lung function either alone or combined with conventional lung function testing in a wide range of pulmonary disorders.

Participation eligibility

Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. There is no guarantee that every individual who qualifies and wants to participate in a trial will be enrolled. Contact the study team to discuss study eligibility and potential participation.

Inclusion Criteria:

Aim 1b:

  • Pediatric patients, accompanied by parent or legal guardian

Aim 2:

  • Adult patients with normal spirometry and MMRC > 0
  • Adult patients with the non-specific pattern and MMRC > 0
  • Adult and pediatric patients with CF
  • Adult patients with PCD
  • Adult lung transplant patients  

Exclusion Criteria:

  • Pediatric patients with no legal guardian available for consenting purposes
  • Physical or cognitive conditions that may not allow the patient to perform the maneuvers outlined

Note: Other protocol defined Inclusion/Exclusion Criteria may apply.

Eligibility last updated 07/25/2024. Questions regarding updates should be directed to the study team contact.

 

 

 

Participating Mayo Clinic locations

Study statuses change often. Please contact the study team for the most up-to-date information regarding possible participation.

Mayo Clinic Location Status Contact

Rochester, Minn.

Mayo Clinic principal investigator

Alexander Niven, M.D.

Contact us for the latest status

Contact information:

Jodi Mahon

(507) 293-0694

Mahon.Jodi@mayo.edu

More information

Publications

Publications are currently not available

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CLS-20572573

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