Status: Not yet recruiting
Post-Market Clinical Follow-Up Study of the Solo+ Tympanostomy Tube Device
The purpose of this project is to collect information from the doctor notes about the use of the device, to monitor the tubes after surgery, and collect information from patients and parents/guardians about their views on the procedure. Since the device became available in Europe, it is important to collect information from both patients planned for the procedure (prospective) and those who already underwent the procedure (retrospective) to have collect as much data as possible.
Participants needed: 160
Trial details
Age: 6+Biological sex: AllType: ObservationalSponsor: AventaMed DACUpdated: Jun 19, 2025
Eligibility criteria
Subject and/or Parent/Guardian is able to understand the information document an... [+1]
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