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. 2021 Oct 12;2021(10):CD013379. doi: 10.1002/14651858.CD013379.pub2

Blumenfeld 2012.

Methods Parallel‐group randomised controlled trial
Participants Inclusion criteria: people with a tracheostomy, naive to a speaking valve, and with dysphagia.
Interventions Intervention
Received a speaking valve used for 45 minutes/day and during therapy.
Control
Received an inner cannula only.
Outcomes
  • Penetration aspiration scale.

  • Secretion rating.

Notes Unable to identify published study.