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Completed

NCT Number: NCT04404036

SinuSonic for ETD and Facial Pain: Acoustic Vibration + Oscillating Expiratory Pressure

This study was originally designed with three aims: (1) healthy controls to assess nasal nitric oxide, (2) adults with Eustachian Tube Dysfunction (ETD), and (3) adults with facial pain/pressure. However, only the ETD cohort (Aim 2) was initiated and enrolled. During study conduct, additional symptom and pain assessments (including MPQ-SF and mBPI-sf) were collected in the ETD cohort for exploratory purposes. All results in this record reflect ETD cohort participants who used the SinuSonic device twice daily for 6 weeks.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Sinus Center - Medical Univesity of South Carolina

Charleston, South Carolina, 29425, United States

About this study

The original protocol included three planned cohorts:

  • Aim 1 - healthy controls for exhaled nasal nitric oxide (NO) testing;
  • Aim 2 - adults with Eustachian Tube Dysfunction (ETD) to evaluate safety and efficacy;
  • Aim 3 - adults with facial pain/pressure.

Only Aim 2 (ETD cohort) was opened to enrollment. Aims 1 and 3 were not initiated, and no participants were enrolled in those cohorts.

During study conduct, several patient-reported outcome measures originally associated with Aim 3 (MPQ-SF and mBPI-sf) were also administered to the ETD cohort for exploratory symptom profiling. Therefore, the Results section includes ETD-specific measures (ETDQ-7, ETD Symptom VAS, tympanogram) as well as pain-related measures for participants enrolled in the ETD cohort. All analyses derive exclusively from the ETD cohort participants (N=29 with baseline data).

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

AIM 1

Inclusion criteria

  • Adults 18 years or older with no symptoms of URI, ETD or other ENT conditions

Exclusion criteria

  • Sinonasal or ear surgery within last 3 months (including balloon ET dilation)
  • Any ENT condition that may impact upper airway to include sinusitis, otitis, or allergies
  • Upper respiratory illness within last 2 weeks
  • Topical decongestant use in last week
  • Current nasal crusting or ulceration on rhinoscopy
  • History of severe nose bleeding within last 3 months
  • Known pregnancy
  • Allergic sensitivity to silicone or any other component of device
  • Inability to read and understand English
  • Inability to perform treatment due to underlying medical condition

AIM 2

Inclusion:

  • Adults 18 years or older with diagnosis of ETD by an otolaryngologist
  • ≥6 months of symptoms duration
  • ≥3 ETD symptoms (ear pressure, feeling that ears are clogged, cracking/popping of ears, muffled hearing, tinnitus)
  • ETDQ-7 score ≥ 3
  • Audiogram within the last year

Exclusion:

  • Sinonasal or ear surgery within last 3 months (including balloon ET dilation)
  • Indwelling ear tubes
  • Tympanic membrane perforation
  • Hx of cholesteatoma, mastoidectomy, tympanoplasty, or ossicular chain reconstruction
  • Patulous ET
  • Hx of Meniere's disease
  • Moderate or severe nasal valve collapse
  • Grade 3-4 polyps
  • Upper respiratory illness within last 2 weeks
  • Topical decongestant use in last week
  • Current nasal crusting or ulceration on rhinoscopy
  • History of severe nose bleeding within last 3 months
  • Known pregnancy
  • Allergic sensitivity to silicone or any other component of device
  • Inability to read and understand English
  • Inability to perform treatment due to underlying medical condition

AIM 3

Inclusion:

  • Adults 18 years or older who complain of facial pain or pressure
  • ≥3 months of symptoms duration (can be intermittent)
  • Pain/pressure VAS score ≥ 5

Exclusion:

  • Sinonasal surgery within the last 3 months
  • Grade 3-4 polyps
  • Upper respiratory illness within last 2 weeks
  • Topical decongestant use in last week
  • Current nasal crusting or ulceration on rhinoscopy
  • History of severe nose bleeding within last 3 months
  • Known pregnancy
  • Allergic sensitivity to silicone or any other component of device
  • Inability to read and understand English
  • Inability to perform treatment due to underlying medical condition

Treatment and study plan

SinuSonic Device

Device

A medical device that combines acoustic vibration with oscillating expiratory pressure.

Primary outcomes

  1. Eustachian Tube Dysfunction (ETD) Symptom Visual Analog Scale (VAS) - Total Score

    Time frame: 6 weeks (baseline to 6-week follow-up)

    Five ETD symptoms (ear pressure, ear clogging, cracking/popping, muffled hearing, tinnitus) are each rated on a 10-cm line from 0 = "Not troublesome" to 10 = "Worst thinkable/troublesome." The total score is the sum of all five items (range 0-60). Higher scores indicate worse symptoms.

Secondary outcomes

  1. McGill Pain Questionnaire - Short Form (MPQ-SF) Total Score

    Time frame: 4 weeks

    The MPQ-SF includes 15 descriptors scored from 0 (none) to 3 (severe). Total score ranges from 0-45. Higher scores indicate worse pain.

  2. Modified Brief Pain Inventory - Short Form (mBPI-sf): Worst Pain

    Time frame: 4 weeks

    Participants rate worst pain on an 11-point scale from 0 = "No pain" to 10 = "Worst pain imaginable." Higher scores indicate worse pain.

Sponsors and collaborators

Lead sponsor

Medical University of South Carolina

Other

Registry information

Official study title

Treatment of Eustachian Tube Dysfunction (ETD) and Facial Pain With Combined Acoustic Vibration and Oscillating Expiratory Pressure

Important dates

Study start
2020
Primary completion
2023
Study completion
2023
First posted
May 27, 2020
Registry last updated
Feb 13, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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