CompletedNCT05685186

A Longitudinal, Observational Study of Primary Ciliary Dyskinesia in Adults

Studying Primary ciliary dyskinesia

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Key facts

Sponsor
ReCode Therapeutics
Principal Investigator
Priya Ryali
ReCode Therapeutics
Intervention
Spirometry(diagnostic_test)
Enrollment
31 enrolled
Eligibility
18-60 years · All sexes
Timeline
20232025

Study locations (1)

Collaborators

University of North Carolina, Chapel Hill

Primary source

Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.

Open NCT05685186 on ClinicalTrials.gov

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