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Clinical trial

This Study Will be a Prospective, Non-randomized Evaluation of the Change Between Preoperative and Postoperative Outcomes for Those Who Receive the BioDuct® Device Meniscal Repair Device.

NCT01270919 is registered in ClinicalTrials.gov with Stryker Orthopaedics as lead sponsor.

NCT NCT01270919
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Registry record

As filed in ClinicalTrials.gov.

Title
This Study Will be a Prospective, Non-randomized Evaluation of the Change Between Preoperative and Postoperative Outcomes for Those Who Receive the BioDuct® Device Meniscal Repair Device.
Lead sponsor
Stryker Orthopaedics
Phase
Not applicable
Overall status
Terminated
Start date
November 30, 2010
Completion date
May 31, 2011
Enrollment
1 (actual)
Sites
3

Conditions

As the registry lists them; a condition with its own page is linked.

knee meniscus tear