RecruitMe Clinical Trial

A prospective, single blinded, multi-center, randomized, controlled, pivotal study to assess the safety and effectiveness of the InSpace device for treatment of full thickness Massive Rotator Cuff Tears
A study assessing the study device, InSpace device, for treatment of massive rotator cuff tears
Sponsor:Ortho-Space Ltd.
Enrolling:Male and Female Patients
Study Length:48 Months
Clinic Visits:8
Age Range:Between 40 and years old
IRB Number:AAAR1045
U.S. Government ID:NCT02493660
Contact: William Levine: 212-305-0998 / wnl1@cumc.columbia.edu
Additional Study Information:

The study is designed to evaluate the safety and effectiveness of the InSpace device as a primary surgical treatment for a full thickness Massive Rotator Cuff Tears (MRCT) in comparison to Partial Repair of a full thickness MRCT performed during an arthroscopic procedure.

Do You Qualify?
Do you have a full-thickness or complete tear or your rotator cuff?YesNo
Have you had previous shoulder surgery in the past 1 year?YesNo
Is your condition affecting both shoulders and rotator cuff repair is scheduled or to be scheduled?YesNo
You may be eligible for this study

Place Holder




Who Can I Contact?
For more information, please contact:

William Levine

wnl1@cumc.columbia.edu

212-305-0998

YesNoNo3