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Clinical trial

A Randomized, Two-arm, Prospective, Subject Blind Study to Assess the Safety and Efficacy of InSpace™ Device in Comparison to Full Thickness Massive Rotator Cuff Repair in Subjects Scheduled for a Repair Surgery.

NCT02208440 is registered in ClinicalTrials.gov with OrthoSpace Ltd. as lead sponsor.

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Registry record

As filed in ClinicalTrials.gov.

Title
A Randomized, Two-arm, Prospective, Subject Blind Study to Assess the Safety and Efficacy of InSpace™ Device in Comparison to Full Thickness Massive Rotator Cuff Repair in Subjects Scheduled for a Repair Surgery.
Lead sponsor
OrthoSpace Ltd.
Phase
Not applicable
Overall status
Terminated
Start date
July 31, 2014
Completion date
January 31, 2019
Enrollment
14 (actual)
Sites
1

Conditions

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

full-thickness rotator cuff tear