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:
2026-03-26 @ 3:15 PM
Ignite Modification Date:
2026-03-26 @ 3:15 PM
NCT ID:
NCT07355166
Eligibility Criteria:
Inclusion Criteria:
* Patients undergoing reconstruction of primary ACL tear
Exclusion Criteria:
* Concurrent ligamentous injuries requiring surgical intervention
* Full thickness cartilage injury requiring discrete surgical intervention
* Chronic opioid use
* Significant hepatic disease (Child/Pugh C)
* Women who are pregnant or breastfeeding
* Women of childbearing age using hormonal contraceptives containing progestins other than levonorgestrel and norethindrone
* Allergies or intolerance to any study medications
* Inability to complete ePROs (due to literacy or infirmity)
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT07355166
Study Brief:
Protocol Section:
NCT07355166