Clin2
NCT05479643Possibly a fitNot yet recruiting

Personal voice restoration device for people after laryngectomy

DysphoniaAphonia

Part of Brain & nervous system, Ear, nose & throat, Lungs & breathing clinical trials.

This study tests a personalized device designed to help restore voice function for people who have lost or severely weakened their voice after laryngectomy. You may be invited if you are an adult with specific voice problems, or (in a separate group) if you are healthy and have normal voice.

Summary written for real people, not researchers, by Clin2.

Phase
N/A
Enrollment
100 people
Ages
18 years to 110 years
Study type
Interventional

Who can take part

  • You must be 18 years or older.
  • You must belong to one of two groups: healthy volunteers with normal voice, or someone with severe voice problems (aphonia or dysphonia).
  • If you have voice problems, you need documentation of severe dysphonia/aphonia or a GRBAS score above 0 (a checklist rating voice quality).
  • If you’re a healthy volunteer, you cannot have any voice impairment (any voice problem).
  • If you have voice problems, you must not have face muscles that are entirely paralyzed.

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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