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Clinical Trials/NL-OMON24952
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.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
2 years ago
Study Type
Interventional

Investigators

Sponsor
Afdeling OrthopaedieHAGA HospitalSportlaan 6002566MJ, Den Haag, Nederland

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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