NL-OMON24952
Recruiting
Not Applicable
Difference in pain and functional outcome after arthroscopic debridement vs debridement and biodegradable implanted balloon for irreparable rotator cuff tears.
Afdeling OrthopaedieHAGA HospitalSportlaan 6002566MJ, Den Haag, Nederland0 sites104 target enrollmentTBD
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Shoulder debridement biodegradable balloon rotator cuff tear Schouder debridement , bio-oplosbare ballon, rotator cuff herstel
- Sponsor
- Afdeling OrthopaedieHAGA HospitalSportlaan 6002566MJ, Den Haag, Nederland
- Enrollment
- 104
- Status
- Recruiting
- Last Updated
- 2 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Subject has an irreparable supra\- and infraspinatus tendon tear confirmed by ultrasound or MRI and is according to the Orthopaedic Surgeon a suitable candidate for debridement.
- •The symptoms of the subjects are existing for at least twelve months, despite conservative treatment, including physiotherapy, subacromial infiltration with corticosteroids or anti\-inflammatory drugs.
Exclusion Criteria
- •Subject is not able to complete the daily questionnaires in Dutch.
- •Subject, in the opinion of the investigator, is not able to understand this investigation and is not willing and able to perform all study procedures and co\-operate with investigational procedures.
Outcomes
Primary Outcomes
Not specified
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