A pilot study of evaluating the effect of an electronic earwax removal device

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

CRIS

Registry ID

KCT0007429

Enrollment

Registered

2022-06-22

Start date

2022-05-19

Completion date

Unknown

Last updated

2022-06-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Others(electronic earwax removal device) : After explaining how the OtoBlow works to the participant, using the Otoblow on one side and a cotton swab on the other side, the participant removes earwax

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Adults 20 years of age or older with wet-type or close to wet-type earwax and no underlying diseases.

Exclusion criteria

Exclusion criteria: A) Under the age of 20 B) If you have an underlying disease (cognitive dysfunction, immune system disease, vulnerable to infection, cancer) C) Cases where there is a high possibility of side effects of ear wax remover due to abnormalities in the external eardrum or infection findings, etc. due to eardrum endoscopy. D) Vulnerable study subjects (pregnant women, students, adults with impaired consent skills, etc.)

Design outcomes

Primary

Measure	Time frame
An eardrum endoscope, tympanometry	—

Secondary

Measure	Time frame
Assessment of satisfaction through questionnaire	—

Countries

Korea, Republic of

Contacts

Public ContactKieun Lee

Seoul National University Hospital

leeki0819@snu.ac.kr+82-2-3668-7380

Outcome results