drugset / Trial / NCT02141191

A Study of Lung Clearance After Hypertonic Saline Delivery Using the tPAD Device

NCT02141191

Phase 1 Completed 12 enrolled University of Pittsburgh Parion Sciences · collab
RandomizedCrossoverOpen-labelTreatment

Summary

The primary objective of this study is to determine whether a single overnight, eight-hour administration of a 7% NaCl solution delivered by the Parion Sciences transnasal Pulmonary Aerosol Delivery (tPAD) device has a significant effect on mucociliary clearance in subjects with cystic fibrosis, as compared to no treatment. This study will be conducted at the University of Pittsburgh Medical Center.

Timeline

Start
2014-06
Primary completion
2015-10
Completion
2015-10

Drugs

EvaluationDrugModalityDoseRoute
Subject Hypertonic saline Unknown 7 % Intranasal

Indications