MedTrace Logo

Neurogenic Dysphonia/Dysphagia Registry

NCT02493491 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 146

Last updated 2016-09-09

No results posted yet for this study

Summary

The Neurogenic Dysphonia/Dysphagia Registry is designed to be purely observational (i.e. non-interventional, exploratory). Patient data collected from the registry is expected to be consistent with any information which can be obtained during usual care of patients with dysphonia/dysphagia treated with vocal fold augmentation.

Conditions

  • Neurogenic Dysphonia
  • Neurogenic Dysphagia

Sponsors & Collaborators

  • Carelon Research

    collaborator OTHER

  • Cmed Clinical Services

    collaborator OTHER

  • Merz North America, Inc.

    lead INDUSTRY

Principal Investigators

  • Scott Sykes, MD · Merz North America, Inc.

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-06-30
Primary Completion
2016-08-31
Completion
2016-09-30

Countries

  • United States

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02493491 on ClinicalTrials.gov