ENTegral Artificial Larynx Clinical Trial
NCT01948219 · Status: TERMINATED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 2
Last updated 2018-04-05
Summary
The objective of this clinical study is to evaluate the feasibility, safety and efficacy of the ENTegral Artificial Larynx (AL) in patients indicated for total laryngectomy.
Conditions
- Total Laryngectomy
Interventions
- DEVICE
-
ENTegral Artificial Larynx implant
Sponsors & Collaborators
-
ProTiP Medical
lead INDUSTRY
Study Design
- Allocation
- NA
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2014-10-31
- Primary Completion
- 2016-06-30
- Completion
- 2016-06-30
Countries
- Belgium
- France
Study Locations
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