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InSpace™ System in Comparison to Best Repair of Massive Rotator Cuff Tear

Not Applicable
Terminated
Conditions
Rotator Cuff Tear
Interventions
Device: InSpace™ system
Procedure: Best Repair of torn Rotator Cuff
Registration Number
NCT02211183
Lead Sponsor
OrthoSpace Ltd.
Brief Summary

This is a post-marketing study to further assess the safety and effectiveness of the InSpace™ device implantation in comparison to surgical repair of full thickness Massive Rotator Cuff Tear .

Detailed Description

The effectiveness will be assessed by comparing the scores of the ASES, Constant and Quick DASH outcome questionnaires with respect to pain reduction, improvement of activity of daily living (ADL) and improvement of range of motion (ROM).

Recruitment & Eligibility

Status
TERMINATED
Sex
All
Target Recruitment
4
Inclusion Criteria
  • Age 40 or older.
  • Positive diagnostic imaging of the affected shoulder indicating full thickness Massive RCT (according to Cofield classification) or long involving more than one tendon.
  • Persistent pain and functional disability of the affected shoulder for at least 3 months.

Main Exclusion Criteria :

  • Known allergy to the balloon material (copolymer of PLA and -θ-caprolactone).
  • Evidence of significant osteoarthritis or cartilage damage in the shoulder
  • Evidence of gleno-humeral instability
  • Previous surgery of the shoulder in the past 2 years, excluding diagnostic arthroscopy
  • Evidence of major joint trauma, infection, or necrosis in the shoulder
  • Partial-thickness tears of the rotator cuff
Exclusion Criteria

Not provided

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
InSpace™ systemInSpace™ systemSubjects will undergo surgical intervention (usually arthroscopy or mini invasive) of debridement, acromioplasty if deemed necessary with or without long head of biceps tenotomy, and placement of the InSpace™ system.
Best Repair of torn Rotator CuffBest Repair of torn Rotator CuffSubjects will undergo surgical intervention (usually arthroscopy) to perform debridement, acromioplasty if deemed necessary, long head of biceps tenotomy, and at least partial repair.
Primary Outcome Measures
NameTimeMethod
The change in Shoulder Score from baselinebaseline and 6 months
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Fundacion Jimenez Diaz

🇪🇸

Madrid, Spain

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