Balloon Dilation in Selected Subjects With Refractory Eustachian Tube Dysfunction

Eustachian Tube Dysfunction Clinical Trial

Official title:

Balloon Dilation in Selected Subjects With Refractory Eustachian Tube Dysfunction

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02114762
• Other study ID #: PRO13120437
• Secondary ID: R21DC013167
• Status: Completed
• Phase: N/A
• First received: April 7, 2014
• Last updated: September 6, 2017
• Start date: April 2014
• Est. completion date: April 30, 2017

Study information

• Verified date: September 2017
• Source: University of Pittsburgh
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This study evaluates the usefulness and safety of using a balloon to dilate (make larger) the Eustachian tube in adults who have middle-ear disease due to Eustachian tube dysfunction.

Description:

The Eustachian tube is a biological tube that connects the back of the nose to the middle ear. It is usually closed but needs to be actively opened by the action of certain muscles during swallowing, yawning, and other activities which keeps the air pressure in the middle ear (the part of the ear behind the eardrum) the same as the air pressure in the environment. If the Eustachian tube does not open during swallowing, the middle-ear pressure progressively decreases and persons may have the feeling of a "stuffed up" and/or "full" middle ear, may have difficulty hearing and/or may develop fluid in their middle ear.

The usual treatment for a Eustachian tube that does not open well is to insert a tiny tube (called a ventilation or tympanostomy tube) into the eardrum to keep the air pressure in the middle ear the same as in the environment. However, those tubes naturally "fall out" over time, and if the Eustachian tube opening function had not improved while they were in place, new tubes will need to be inserted. In the past few years, doctors in the U.S. and Europe described a simple procedure called "balloon dilation of the Eustachian tube" (BDET) or "balloon tuboplasty" that they believe corrects the underlying cause of Eustachian tube dysfunction and resolves its symptoms, signs and consequences. For that procedure, a tiny balloon is inserted into the Eustachian tube, inflated to physically open the Eustachian tube, deflated and then removed. Doctors who have used the method in adults and children with symptoms of Eustachian tube dysfunction reported that BDET is safe and causes a short-term and, perhaps, a long-term resolution of symptoms. However, no one has measured Eustachian tube function before and after the procedure, and it is not known if BDET truly improves that function or not, and if so, how that function is changed.

In this study, we will enroll adult subjects with a tympanostomy tube inserted into at least one eardrum or a chronic perforation in at least one eardrum for physician-diagnosed Eustachian tube dysfunction or middle-ear fluid and document the presence/absence of measurable Eustachian tube dysfunction using standard tests. If present, we will determine if the Eustachian tube dysfunction improves after medical treatment of other diseases known to cause Eustachian tube dysfunction. If the Eustachian tube dysfunction does not significantly improve, we will perform the BDET procedure and measure the change in Eustachian tube function at different times after the procedure.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 13
• Est. completion date: April 30, 2017
• Est. primary completion date: November 23, 2016
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 50 Years

Eligibility

Inclusion Criteria:

• has functional ventilation tube or a chronic perforation in at least one ear;

• history of Eustachian tube dysfunction and/or otitis media with effusion;

• history of middle-ear effusion at least once;

• otherwise healthy except for possible gastro-esophageal reflux disease (GERD), allergies, sinusitis;

• BMI of less than 35;

• no history of difficult intubation;

• no known family history of malignant hyperthermia.

Exclusion Criteria:

• history of adverse reaction to any study-related medication and a suitable alternative is not available;

• current or past history of cancer;

• current or past history of vestibular pathology or cranial base surgery;

• craniofacial dysmorphology (examples: down syndrome, cleft palate);

• pregnancy or "at risk" and not using contraception;

• patulous Eustachian tube;

• non-patent nasal cavity;

• adenoids that block the Eustachian tube orifice;

• blood pressure greater than 140/90;

• had experimental drug or procedure in the previous 3 months;

• allergic to eggs, egg products, soy, or soy products;

• previously underwent balloon dilation of the Eustachian tube.

Related Conditions & MeSH terms

• Eustachian Tube Dysfunction

Intervention

Procedure:
• Balloon dilation of the Eustachian tube
Insert a balloon into one Eaustachian tube and inflate it for up to one minute. The balloon is then removed.

Locations

Country	Name	City	State
United States	Children's Hospital of Pittsburgh of UPMC	Pittsburgh	Pennsylvania

Sponsors (2)

Lead Sponsor	Collaborator
University of Pittsburgh	National Institute on Deafness and Other Communication Disorders (NIDCD)

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	video-endoscopy	ability of video-endoscopy to diagnose anatomic cause of eustachian tube dysfunction	entry visit
Primary	Eustachian tube function testing	opening pressure, closing pressure, passive resistance	1 month post-operatively
Secondary	Eustachian tube function testing	opening pressure, closing pressure, passive resistance	3 months post-operatively
Secondary	Eustachian tube function testing	opening pressure, closing pressure, passive resistance	6 months post-operatively
Secondary	Eustachian tube function testing	opening pressure, closing pressure, passive resistance	4 weeks after beginning medical treatment