Balloon Dilation of the Eustachian Tube (BDET)

Sunnybrook Health Sciences Centre

Status

Terminated

Conditions

Eustachian Tube Dysfunction

Treatments

Device: Balloon dilation of the eustachian tube

Study type

Interventional

Funder types

Other

Identifiers

NCT05270031

3156

Details and patient eligibility

About

In this study, patients with dysfunction of the eustachian tube will be included. They will be randomized to one of two treatment groups.

balloon dilation of the eustachian tube or
nasal saline Patients will undergo follow-up for one year and will be able to crossover to the treatment arm after three months

Full description

Patients will eustachian tube dysfunction will be asked to participate in the study.

They will be randomized to one of two groups

group 1 - surgical dilation of the eustachian tube in general anaesthesia

group 2 - daily nasal saline spray, twice a day

Regular Follow up with Tympanogram and Questionnaire

After three months patient in the control group (nasal saline) can switch in the intervention group.

Eustachian tube dilation will be carried out with a Health Canada and FDA approved device, usually used for endovascular balloon dilation. It has the same size and pressure properties as the eustachian tube dilation device and has shown a good safety profile in a previous preclinical and clinical pilot study.

Enrollment

15 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

≥18 years old (of both sexes)
Diagnosed with persistent obstructive eustachian tube dysfunction (OETD) for at least 3 months prior to enrolment uni- and/or bilateral

Diagnosis (both required):

i. Persistent OETD symptoms assessed by Eustachian Tube Dysfunction Questionnaire (ETDQ-7) with overall score of ≥3 (moderate to severe symptoms) for 3 months or more prior to enrollment.

ii. Refractory to medical therapy (minimum of 4 weeks of daily intranasal steroid spray or one completed course of an oral steroid within 3 months before study enrollment).

Exclusion criteria

Patulous eustachian tube
Prior eustachian tube intervention
Presence of myringotomy ventilation tube or a tympanic membrane perforation
Active chronic or acute otitis media
Chronic otitis media with cholesteatoma
Fluctuating sensorineural hearing loss or Meniere's disease
Chronic rhinosinusitis, allergies, or reflux disease not controlled with medication
History of head or neck surgery within 3 months
Prior radiation to the head and neck
Active temporomandibular joint disorders
Cleft palate or Craniofacial syndrome
Cystic fibrosis or Ciliary dysmotility syndrome or Systemic immunodeficiencies
Active acute upper respiratory infection
Nasal endoscopy with evidence of anatomic conditions that would prevent transnasal access to the Eustachian tube
CT temporal bone scan with evidence of carotid artery dehiscence, superior semicircular canal dehiscence, or extrinsic eustachian tube compression
Patient unable to follow protocol for any reason