CompletedPhase 2NCT01883531

Crossover Trial Determining the Efficacy of Dry Powder Mannitol to Improve Lung Function in Subjects Aged 6-17 Years

Studying Cystic fibrosis

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Key facts

Sponsor
Syntara
Principal Investigator
Christiane De Boeck
UZ Leuven, Belgium
Intervention
Inhaled Mannitol(drug)
Enrollment
95 enrolled
Eligibility
6-17 years · All sexes
Timeline
2013 – 2015

Study locations (1)

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 NCT01883531 on ClinicalTrials.gov

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