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XprESS ET Registry

NCT04136977 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 169

Last updated 2020-09-30

No results posted yet for this study

Summary

A prospective, multicenter, registry of patients undergoing balloon dilation of the Eustachian tubes (ET).

Conditions

  • Eustachian Tube Dysfunction

Interventions

DEVICE

Eustachian tube dilation

Unilateral or bilateral balloon dilation of the Eustachian tube using the FDA-cleared XprESS ENT Dilation System

Sponsors & Collaborators

  • North American Science Associates Ltd.

    collaborator NETWORK

  • Entellus Medical, Inc.

    lead INDUSTRY

Principal Investigators

  • Edward D McCoul, MD, PhD · Ochsner Health System, New Orleans, LA

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-06-05
Primary Completion
2020-08-28
Completion
2020-08-28
FDA Device
Yes

Countries

  • United States

Study Locations

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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 NCT04136977 on ClinicalTrials.gov