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Clinical Trials/NCT05762497
NCT05762497
Completed
Not Applicable

Pilot Feasibility Study of a Moldable Peristomal Adhesive for Pulmonary and Speech Rehabilitation After Total Laryngectomy

Fondazione Policlinico Universitario Agostino Gemelli IRCCS1 site in 1 country10 target enrollmentJuly 1, 2022

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Laryngectomy; Status
Sponsor
Fondazione Policlinico Universitario Agostino Gemelli IRCCS
Enrollment
10
Locations
1
Primary Endpoint
Investigation about product performance
Status
Completed
Last Updated
3 years ago

Overview

Brief Summary

Loss of voice is one of the greater consequences of total laryngectomy. The voice prosthesis allows the patients to speak again in a very short time but forces them to use one hand when speaking. In order to reduce this discomfort and to allow "hands-free" speaking, an Automatic Speaking Valve (ASV) has been designed which is positioned on a peristomal adhesive.

Peristomal adhesives, however, tend to detach under the influence of mucus, cough, or phonatory pressure. Consequently, the current regular use of the automatic speaking valve in laryngectomees is very low. As a possible solution, Atos Medical AB has developed a moldable peristomal adhesive made of a thermoplastic elastomer, which becomes transparent and moldable when heated and facilitates precise contouring in situ. As the material cools, it loses its malleability but retains the integrity of the molded shape.

The expectation was that the moldable adhesive would provide a better individual fit and therefore longer fixation (especially when using the ASV).

To study the feasibility of this device, 10 total laryngectomized patients were asked to use the new moldable peristomal adhesive for two weeks in conjunction with their normal daily routine for adhesive application and removal, and speech rehabilitation.

Registry
clinicaltrials.gov
Start Date
July 1, 2022
End Date
December 27, 2022
Last Updated
3 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Parrilla Claudio

Principal Investigator

Fondazione Policlinico Universitario Agostino Gemelli IRCCS

Eligibility Criteria

Inclusion Criteria

  • Have undergone total laryngectomy
  • Over the age of 18
  • voice prosthesis user
  • Experience in the use of adhesive and HMEs
  • At least 3 months after total laryngectomy
  • At least 6 months after the end of adjuvant radiotherapy
  • Signature of the informed consent

Exclusion Criteria

  • Medical issues that prevent the use of HMEs and/or adhesives
  • Recurrent or metastatic active disease
  • Reduced mobility of the arms and/or hands
  • Inability to understand the information and/or to provide informed consent
  • Insufficient cognitive ability to handle HME or moldable adhesive

Outcomes

Primary Outcomes

Investigation about product performance

Time Frame: 2 weeks

Duration of hands-free speech \[hours/day\]

Secondary Outcomes

  • Parameters were expected to influence product performance and patient preference(2 weeks)

Study Sites (1)

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