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Clinical trial

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

NCT01890733 is registered in ClinicalTrials.gov with OrthoSpace Ltd. as lead sponsor.

NCT NCT01890733
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Registry record

As filed in ClinicalTrials.gov.

Title
A Randomized, Two-arm, Prospective, Subject Blind Study to Assess the Efficacy and Safety of InSpace™ Device in Comparison to Massive Rotator Cuff Repair in Subjects Scheduled for a Repair Surgery.
Lead sponsor
OrthoSpace Ltd.
Phase
Not applicable
Overall status
Terminated
Start date
September 30, 2012
Completion date
September 30, 2015
Enrollment
5 (actual)
Sites
1

Conditions

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

full- thickness massive rct (mrct) of at least 5 cm in diameter including fatty infiltration grade iii or iv