XprESS ET Registry

Status Completed

Clinical Trial Summary

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

Clinical Trial Description

This is a prospective, multicenter, single-arm, postmarket registry enrolling up to 300 participants who are planning to undergo balloon dilation of the Eustachian tubes for treatment of chronic/persistent Eustachian tube dysfunction (ETD). Procedural information will be collect as well as efficacy and safety data through 6 months post procedure. ;

Study Design

Related Conditions & MeSH terms

Eustachian Tube Dysfunction

Clinical Trial Details

NCT number	NCT04136977
Study type	Observational [Patient Registry]
Source	Entellus Medical, Inc.
Contact
Status	Completed
Phase
Start date	June 5, 2018
Completion date	August 28, 2020

View Details

See also
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