Clinical Trials Directory

Trials / Completed

CompletedNCT00942903

Short-term Clinical Feasibility of the Provox XtraHMEs for Pulmonary Rehabilitation After Total Laryngectomy

Phase 1 Study. Short-term Feasibility of the Next Generation Provox HMEs for Pulmonary Rehabilitation After Total Laryngectomy

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
20 (actual)
Sponsor
Atos Medical AB · Industry
Sex
All
Age
21 Years
Healthy volunteers
Not accepted

Summary

This study is a short term feasibility study that aims to investigate patient satisfaction with and performance of new Provox Xtra HME in 20 laryngectomized patients. Aspects that are considered are for example performance for stoma occlusion, speaking, breathing, appearance, compliance, and short-term impact on pulmonary symptoms.

Conditions

Interventions

TypeNameDescription
DEVICEProvox Xtra HMEHeat and Moisture Exchanger for pulmonary Rehabilitation after total laryngectomy

Timeline

Start date
2009-07-01
Primary completion
2009-08-01
Completion
2009-08-01
First posted
2009-07-21
Last updated
2010-10-22
Results posted
2010-08-30

Locations

1 site across 1 country: Netherlands

Source: ClinicalTrials.gov record NCT00942903. Inclusion in this directory is not an endorsement.

Short-term Clinical Feasibility of the Provox XtraHMEs for Pulmonary Rehabilitation After Total Laryngectomy (NCT00942903) · Clinical Trials Directory