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Clinical Trial

A Randomized Trial Comparing Routine Use of the ActiValve to Standard Voice Prostheses

NCT: NCT07369050 · NOT_YET_RECRUITING

NCT IDNCT07369050
StatusNOT_YET_RECRUITING
Start Date2026-12-01
Completion2030-09-01
SponsorM.D. Anderson Cancer Center (OTHER)
First posted
Last updated

Brief Summary

The goal of this clinical research study is to learn if regular use of Provox® ActiValve® by patients after a total laryngectomy with TEP can decrease the number of VP device replacements needed annually.

Official Source

View on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov API. For the most current status, refer to the official record.

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