Total Laryngectomy Clinical Trial
Official title:
Amendment on Phase 1 Trial N07VEG "Assessment of a Next Generation Indwelling Provox Voice Rehabilitation System (Vega)". Amendment 3: Long-term Use of the Provox Vega
The purpose of this study was to investigate the long-term feasibility of the new Provox Vega 22.5 voice prosthesis (outer diameter of 22.5 French) and its insertion system (SmartInserter) in laryngectomized patients who currently use a Provox2 voice prothesis.
Nowadays, many laryngectomized patients use a voice prosthesis to speak. The Provox2 is an
indwelling voice prosthesis that has been on the market since 1997. Recently a new Provox
voice prosthesis has been developed, the Provox Vega. This prosthesis is available in 3
different outer diameters. In this study the device with an outer diameter of 22.5 French is
tested. The Provox Vega 22.5 is the successor of the Provox2 voice prosthesis. Both
prostheses have an outer diameter of 22.5 French.
Outcomes were recorded by means of patient questionnaires and device life.
It is expected that some patients will like the new device (Provox Vega 22.5) better than
the old one (Provox2) because the airflow resistance for speaking of the new prosthesis is
lower when measured in a laboratory.
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Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Supportive Care
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