Post-Market Clinical Follow-Up Study of the Solo+ Tympanostomy Tube Device
NCT: NCT07029997 · RECRUITING
Brief Summary
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.
Frequently Asked Questions
What is Post-Market Clinical Follow-Up Study of the Solo+ Tympanostomy Tube Device?
Post-Market Clinical Follow-Up Study of the Solo+ Tympanostomy Tube Device is a clinical trial registered under NCT07029997. Current status: RECRUITING.
What is the status of NCT07029997?
The current status of NCT07029997 (Post-Market Clinical Follow-Up Study of the Solo+ Tympanostomy Tube Device) is: RECRUITING.
When did Post-Market Clinical Follow-Up Study of the Solo+ Tympanostomy Tube Device start?
Post-Market Clinical Follow-Up Study of the Solo+ Tympanostomy Tube Device started on 2026-05-21.
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Official Source
View on ClinicalTrials.gov →Data sourced from ClinicalTrials.gov API. For the most current status, refer to the official record.