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Completed
NCT05720286
Performance and Safety of the FIXIT® Anchor in Arthroscopic Rotator Cuff Repair
Conditions: Rotator Cuff Injuries
Sex: All
Ages: 18 Years – N/A
Enrollment: 30
Sponsor: Science and biomaterials
Location: France
Summary
Verification of the performance and safety of the first row resorbable threaded anchor FIXIT® in arthroscopic rotator cuff repair Non-interventional, prospective, non-comparative, multi-center study as part of the post-marketing follow-up of devices
Eligibility Criteria
Inclusion Criteria:Patient with broken tendinopathy of the rotator cuffPatient over 18 years oldPatient who has received complete medical information and not objecting to participate in researchSocial insured patientExclusion Criteria:Pregnant or likely to be pregnant, or breastfeedingPatient under guardianshipNon-cooperative patient, who does not want or is unable to follow the post-operative instructions (drug addict or alcoholic patient in particular)
Source: ClinicalTrials.gov (NCT05720286). StuddyBuddy aggregates publicly available trial information.
