Autopsy report · NCT03904420
An Evidence Based Delivery Model of Care for Newly Implanted Adult CI Recipients
Cause of deathRegulatory or ethics
“FDA determination of Fox software as class III medical device, not CDSS.”
Life of this trial
- Registered 1 month after it had already started.
- Ran for about 8 months before it stopped.
- 4 participants enrolled.
- Results were posted on the registry 1 year after it ended.
Vital statistics
- Status
- Terminated
- Phase
- Na
- Sponsor
- Cochlear
- Sponsor type
- Industry
- Conditions
- Sensorineural Hearing Loss, Bilateral
- Interventions
- Clinical Education and Treatment Model; Traditional Model
- Participants
- 4
- Sites
- 2
- Countries
- United States
Look deeper
- The official registry record (the source of truth)
- Record history: every change the sponsor made
- Open it in the database
Everything here comes from the current ClinicalTrials.gov record. The timeline uses the record’s dates; dates marked planned are the sponsor’s plans. The cause of death is an automatic, unverified label. This is research information, not medical advice.