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More info
You can access this
clinical trial
if you have
Pulmonary Diseases
and you are
over 18
years old
The phase for this study is not defined.
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The purpose

In this research, the investigators will asses the effect of BIS monitoring on propofol usage during elective flexible fiberoptic bronchoscopy. The investigators will examine whether use of BIS monitor enables reduction of sedative dose during bronchoscopy. The investigators will also examine whether administration of lower total sedative dose enables prevention of possible complications.

Provided treatments

  • Device: BIS monitor

Locations near you

Unfortunately, there are no recruiting locations near you. Please check the list with all locations below.
Tris trial is registered with FDA with number: NCT01592513. The sponsor of the trial is Rabin Medical Center and it is looking for 80 volunteers for the current phase.
Official trial title:
Effect of BIS Monitoring on Propofol Usage During Elective Bronchoscopy