Tab Title Description
Surgery using the Arthrex PEEK or Biocomposite FastThread Interference Screw for ACL or PCL (PCL at US sites only, Biocomposite screw PCL only) repair or reconstruction.
Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. There is no guarantee that every individual who qualifies and wants to participate in a trial will be enrolled. Contact the study team to discuss study eligibility and potential participation.
Inclusion Criteria:* Subject requires surgery using the Arthrex PEEK Interference Screw for ACL or PCL (PCL at US sites only) repair or reconstruction or the Arthrex Biocomposite Interference Screw for PCL (PCL at US sites only) repair or reconstruction.* Subject is 18 years of age or over.* Subject is not considered a vulnerable subject (i.e. child, pregnant, nursing, prisoner, or ward of the state).* Subject signed informed consent and is willing and able to comply with all study requirements.Exclusion Criteria:* Current bilateral injury of the ACL or PCL.* Injury of the ACL and PCL in the same knee.* Insufficient quantity or quality of bone.* Blood supply limitations and previous infections which may retard healing.* Foreign-body sensitivity.* Any active infection or blood supply limitations.* Conditions that tend to limit the patient's ability or willingness to restrict activities or follow directions during the healing period.* Subjects that are skeletally immature.
Note: Other protocol defined Inclusion/Exclusion Criteria may apply.
Eligibility last updated 12/10/2025. Questions regarding updates should be directed to the study team contact.
Study statuses change often. Please contact the study team for the most up-to-date information regarding possible participation.
Mayo Clinic principal investigator
Kostas Economopoulos, M.D.
Contact us for the latest status
Faviola Trujillo
(480) 342-2906
Contact Ustrujillo.faviola@mayo.edu