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Clinical Trial Summary

The purpose of this study is to evaluate the effect of tobramycin inhalation solution (TIS) once daily compared tot placebo in patients with non-CF bronchiectasis. The primary endpoint is a reduction of exacerbations of the disease during the treatment period. Next to this parameter the investigators expect to show a significant beneficial effect on lung function parameters, QoL, bacterial load of pathogens in sputum and tobramycin resistance.


Clinical Trial Description

See uploaded study protocol ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02657473
Study type Interventional
Source Medical Center Alkmaar
Contact
Status Completed
Phase Phase 2/Phase 3
Start date August 13, 2016
Completion date December 13, 2019

See also
  Status Clinical Trial Phase
Recruiting NCT01822834 - Bronchiectasis and NTM Research Registry
Recruiting NCT04793867 - Regional Phenotyping of CF and Non-CF Bronchiectasis