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 @ 10:48 PM
Ignite Modification Date:
2025-12-24 @ 10:48 PM
NCT ID:
NCT07076069
Eligibility Criteria:
Inclusion Criteria:
* Adults with rotator cuff tears who have failed conservative therapy and undergoing arthroscopic rotator cuff repair.
Exclusion Criteria:
* Patients without capacity to consent for the study
* Patients not able to have local nerve block
* Patients who underwent previous shoulder surgery on the same side, kindling revision rotator cuff repair
* Patients who are unable to record and verbalize their pain level due to altered mental status
* Patients who are unable to tolerate any of the medications included in the multimodal pain regimen or standard pain regimen due to severe allergies or inability to consume medication
* Patients with history of previously diagnosed alcohol or drug abuse, renal impairment, peptic ulcer disease, and gastrointestinal bleeding
* Patients who are pregnant
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT07076069
Study Brief:
Protocol Section:
NCT07076069