Utility of PCD Diagnostics to Improve Clinical Care
Part of paid clinical trials in Nashville, Tennessee.
- Sponsor
- Vanderbilt University Medical Center
- Study ID
- NCT03704207
- Status
- Recruiting
Conditions
- Primary Ciliary Dyskinesia
Eligibility Criteria
- Sex
- ALL
- Age
- 1 Year - N/A
- Healthy Volunteers
- Not accepted
Interventions
- nNO testing — OTHERCollection of already performed clinical data and nNO testing
Study Details
This is a study evaluating the utility of current Primary Ciliary Dyskinesia (PCD) diagnostic tests, including nasal nitric oxide testing.
Key Dates
- Start date
- Jun 1, 2017
- Status verified
- Jun 2025
- Primary completion
- Jun 1, 2028
- Completion
- Jun 1, 2028
Study Design
- Enrollment
- 200 participants (estimated)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- DIAGNOSTIC
Arms
- Other: Nasal Nitric Oxide testing and collection of clinical dataParticipants will have nNO testing is indicated. All participants in this study have some basic clinical data collected at time of enrollment. Participants with a confirmed diagnosis of PCD or in those participants with a working diagnosis of PCD in which ongoing nNO testing is performed have prospective data collection. Some participants have a confirmed diagnosis of PCD by genetics or ciliary biopsy at time of study entry and thus do not need nNO testing, but are followed prospectively with collection of basic clinical data
Primary Outcome Measure
frequency of nNO tests performed [ Time Frame: 3 years ]
Central Contacts
- Michael O'Connor, MD615.343.7617
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Vanderbilt Children's hospital | Nashville | Tennessee | 37232 | Michael O'Connor, MD |
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