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| Name | Class |
|---|---|
| Baxter Healthcare Corporation | INDUSTRY |
Randomized controlled trial on efficacy of single injection or continuous interscalene brachial plexus block on analgesia in patients having outpatient rotator cuff surgery.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Baxter INFUSOR System | Experimental | Regional Analgesia INFUSOR system with Patient Control Module for post-operative analgesia |
|
| Single Injection of Local Anesthetic | Active Comparator | Single injection of 20 ml ropivacaine 0.5% |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Baxter INFUSOR System | Device | Regional Analgesia INFUSOR system with Patient Control Module for post-operative analgesia |
|
| Measure | Description | Time Frame |
|---|---|---|
| Quality of Life | To describe rehabilitation achievement and quality of life during 24-week follow-up after shoulder arthroscopy and rotator cuff repair, and identify any association between type of anesthesia procedure and patients' quality of life | 24 weeks |
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Inclusion Criteria:
Patients who agree to participate in the study will be asked to sign the informed consent and the HIPAA form.
Inclusive criteria are:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Admir Hadzic, MD PhD | St. Luke's-Roosevelt Hospital Center | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| St. Luke's-Roosevelt Hospital | New York | New York | 10025 | United States |
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| Single Injection of Local Anesthetic | Drug | Single injection of 20 ml ropivacaine 0.5% |
|
| ID | Term |
|---|---|
| D000070636 | Rotator Cuff Injuries |
| ID | Term |
|---|---|
| D012421 | Rupture |
| D014947 | Wounds and Injuries |
| D000070599 | Shoulder Injuries |
| D013708 | Tendon Injuries |
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