Utility of Advanced Ultrasound Otoscope In The Diagnosis of AOM

Last updated: September 4, 2025
Sponsor: Baylor College of Medicine
Overall Status: Active - Not Recruiting

Phase

N/A

Condition

Ear Infections (Pediatric)

Otitis (Pediatric)

Otitis Externa (Swimmer's Ear)

Treatment

Advanced Ultrasound Otoscope

Clinical Study ID

NCT06429709
H-50018
  • Ages < 12
  • All Genders

Study Summary

The objective of this study is to collect ultrasound signal information and visual otoscopic images with an engineering prototype device for children scheduled for tympanostomy tube surgery for the purpose of algorithm development.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Newborn to 12 years of age

  • Receiving first set of pressure equalization (PE) tubes, even if coordinated withother procedures such as adenoidectomy

  • Indication for surgery includes recurrent acute otitis media, chronic otitis mediawith effusion, Eustachian tube dysfunction, and/or hearing loss.

Exclusion

Exclusion Criteria:

  • Cholesteatoma, tympanic membrane perforation, myringitis

  • History of PE tube placement or PE tubes currently in place.

Study Design

Total Participants: 300
Treatment Group(s): 1
Primary Treatment: Advanced Ultrasound Otoscope
Phase:
Study Start date:
September 01, 2021
Estimated Completion Date:
December 31, 2026

Study Description

The objective of this study is to collect ultrasound signal information and visual otoscopic images with an engineering prototype device for children scheduled for tympanostomy tube surgery for the purpose of algorithm development.

After informed consent from a parent or guardian is obtained, ultrasound and visual data will be collected for each of the child's ears. The images will be taken with the Advanced Ultrasound Otoscope device. The ear laterality will be noted as well as any infection present in the fluid, non-infected fluid, or normal findings in the middle ear as reported by the surgeon. No identifiable data will be recorded. Each study participant will be given a unique study number that will be linked to the images and middle ear findings. No additional information is gathered including age, sex, name or other PHI. The images and corresponding study data will be stored on a password protected smartphone or tablet as well as on a password protected external hard drive. Other characteristics that will be collected include surgical and lab findings regarding effusion, presence or absence (i.e. effusion). The middle ear fluid which is usually suctioned will be collected in a trap chamber- Tympap- and this collected fluid will be sent to the microbiology laboratory for analysis

Investigators will be collecting ultrasound and visual data from the tympanic membrane. The images the investigators are collecting are optical images of the surface of the tympanic membrane. The waveforms do not traverse the body tissue, the tympanic membrane is a strong reflector, and the signal is returned to the ultrasound transducer for processing the waveform from an analog to a digital signal. The power of the ultrasound signal is 1/1000th of the ultrasound power used for fetal imaging which is considered safe.

Connect with a study center

  • Texas Children's Hospital

    Houston, Texas 77030
    United States

    Site Not Available

  • Texas Children's Hospital

    Houston 4699066, Texas 4736286 77030
    United States

    Site Not Available

Not the study for you?

Let us help you find the best match. Sign up as a volunteer and receive email notifications when clinical trials are posted in the medical category of interest to you.