PF-AtlasClinical Trials › NCT02038803

Efficacy of TOBI Podhaler vs. Tobramycin Inhalation Solution

TOBIpodhaler · Not specified

Registry ID
NCT02038803
Phase
Not specified
Status
Terminated
Drug / intervention
TOBIpodhaler
Sponsor
Rush University Medical Center
Start
2013-10-10
Enrollment
5
Locations
1

About this trial

Inhaled tobramycin is a Cystic Fibrosis Foundation recommended effective treatment for individuals with cystic fibrosis for the management of Pseudomonas aeruginosa airway colonization and improves the FEV1 and reduces the number of acute pulmonary exacerbations of CF. Patients typically use the inhaled tobramycin for a period of 28 days. Unfortunately, the standard nebulizer method for delivering tobramycin inhaled solution (TIS) is time-consuming and may result in missed therapy doses and suboptimal care. A new inhaled formulation and delivery device, the TOBI Podhaler (TPI), an alternative method of administering inhaled Tobramycin will be used and assessed. This new pocket-sized disposable inhaler is maintenance-free, requires no refrigeration or power source, and should greatly increase patient mobility and improve time management.

View NCT02038803 on ClinicalTrials.gov →

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Medical disclaimer. This page summarizes public trial data for NCT02038803 for information only. It is not medical advice, an endorsement, or an offer to enroll. Confirm details on ClinicalTrials.gov and with a qualified physician.