Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 3:32 PM
Ignite Modification Date:
2025-12-24 @ 3:32 PM
NCT ID:
NCT02450292
Eligibility Criteria:
Inclusion Criteria:
* Ages 18-50
* Patients who underwent primary ACL reconstruction performed by one of the study investigators at least 5 years ago
* Isolated ACL tear
* Type of graft used was bone-patellar tendon-bone autograft
* Type of screw used to attach graft to the tibia and/or femur was a BioComposite interference screws (Arthrex, Inc.)
* No degenerative joint disease on preoperative X-rays (\> 50% joint space loss, presence of osteophytes)
Exclusion Criteria:
* Revision ACL reconstructions
* Types of grafts other than bone-patellar tendon-bone autograft were used
* ACL tear with concomitant pathology
* Degenerative joint disease on preoperative X-ray (\> 50% joint space loss, presence of osteophytes)
* Metal or other types of bioabsorbable screws other than BioComposite interference screws (Arthrex, Inc.) were used
* ACL reconstruction performed less than 5 years ago
* Pregnancy
* Greater than Grade 2 laxity of other ligaments
* No additional fixation
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Maximum Age:
50 Years
Study:
NCT02450292
Study Brief:
Protocol Section:
NCT02450292