Autopsy report · NCT01333761

Cardiox Shunt Detection Technology Study

“1)new FDS device design 2)improved Valsalva procedure 3)improved headbands and earpads.”

The sponsor’s own words in the registry.

Life of this trial

• Ran for about 1 year 3 months before it stopped.
• 71 participants enrolled.
• No results are posted on the registry.

Vital statistics

Status

Terminated

Phase

Phase 3

Sponsor

Cardiox Corporation

Sponsor type

Industry

Conditions

Patent Foramen Ovale

Interventions

Cardiox FDS

Participants

71

Sites

7

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.