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:
2025-12-25 @ 3:04 AM
Ignite Modification Date:
2025-12-25 @ 3:04 AM
NCT ID:
NCT03380533
Eligibility Criteria:
Inclusion Criteria:
* Patient diagnosed with rotator cuff injury, regardless of the type of injury.
* Patient undergoing Arthroscopic Rotator Cuff Repair
Exclusion Criteria:
1. Refusal to participate or inability to understand the informed consent process.
2. Inability to understand subjective scales of pain
3. Regular use of narcotics
4. Allergy or intolerance to drugs used in the protocol
5. Consumption of drugs that interact with Buprenorphine (anticholinergics, Atropine, Belladonna, Benztropine, Dicyclomine, Diphenhydramine, Isopropamide, Procyclidine and Scopolamine, Antiarrhythmics, Amiodarone, Disopyramide, Dofetilide, Procainamide, Quinidine and Sotalol.
Anticonvulsants; Carbamazepine, Phenobarbital, Phenytoin and Rifampin)
6. History of previous surgeries in shoulder treated with RAMR
7. Previous neuromuscular deficit
8. Febrile Syndrome
9. Autoimmune or Rheumatologic Disease
10. History of intestinal transit disorders (paralytic ileus)
11. History of alcohol or drug abuse
12. Patients in psychological or psychiatric treatment for anxiety disorders, personality disorders, mood disorders.
Healthy Volunteers:
True
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT03380533
Study Brief:
Protocol Section:
NCT03380533