The objective of this study is to evaluate pre- and intraoperative voice quality, the degree of vocal fold closure and the Maximum Phonation Time (MPT), first determined after temporary APrevent® VOIS implantation and then after permanent existing product implantation.
Age range
18 Years – 80 Years
Sex
ALL
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The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
Change in voice quality by RBH-Scale
Timeframe: pre-surgery, right after temporarily implantation
Change in Glottal closure by Södersten and Lindestad classification
Timeframe: pre-surgery, right after temporarily implantation
Change in maximum phonation time in seconds
Timeframe: pre-surgery, right after temporarily implantation