Autopsy report · NCT01270919
A Prospective, Post-market, Multi-center Feasibility Study of the BioDuct® Meniscal Repair Device
Cause of deathNo reason given
Life of this trial
- Registered 2 months after it had already started.
- Ran for about 6 months before it stopped.
- 1 participant enrolled.
- Results were posted on the registry 3 years 1 month after it ended.
Vital statistics
- Status
- Terminated
- Phase
- Na
- Sponsor
- Stryker Orthopaedics
- Sponsor type
- Industry
- Conditions
- Knee Meniscus Tear
- Interventions
- BioDuct Meniscal Repair Device
- Participants
- 1
- Sites
- 3
- 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.