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NCT02462382 · ClinicalTrials.gov registry record · Phase 4
Efficacy of Continuous Infusion Ropivacaine Interscalene Blocks
A Phase 4 study of Full-thickness Rotator Cuff Tear, sponsored by Orlando Health.
- Completed
- Registry status
- Phase 4
- Development phase
- 51
- Enrollment target
- 1
- Study location
NCT02462382 is a Phase 4 study of Full-thickness Rotator Cuff Tear that has completed, run by Orlando Health. The registered enrollment target is 51 participants. The trial reports 1 study location across 1 state.
The verdict
NCT02462382, a Phase 4 study of Full-thickness Rotator Cuff Tear, has completed, sponsored by Orlando Health.
- COMPLETED
- Registry status
- Phase 4
- Development phase
- 51 participants
- Enrollment target
- 1
- Study location
Study Summary
Arthroscopic rotator cuff repair is a common and painful procedure routinely performed on an outpatient basis. Postoperative pain control regimens can include narcotic pain medicine, non-steroidal anti-inflammatory medications and regional anesthesia such as an interscalene block (ISB). Regional blocks such as ISB can safely provide complete pain relief for the shoulder and upper extremity for eight to twelve hours1. However, the shoulder is still very painful when the block wears off. The purpose of this study is to: 1. Examine the efficacy of continuous infusion scalene block ropivacaine catheters during the first two days after arthroscopic rotator cuff repair. 2. Examine narcotic consumption after continuous infusion scalene block ropivacaine and placebo catheters after arthroscopic rotator cuff repair. 3. Evaluate for any continued pain relief benefit of continuous infusion scalene block ropivacaine catheters during the three days after the infusion catheters have finished.
Conditions Studied
Interventions
- DRUG Saline
- DRUG Ropivacaine
- PROCEDURE Arthroscopic Rotator Cuff Repair
Study Locations (1)
Florida
- Orlando Orthopaedic Center - Orlando
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 51 participants |
| Start Date | 2013-09-01 |
| Est. Completion | 2016-05-20 |
| Phase | Phase 4 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT02462382
The ClinicalTrials.gov registry entry for NCT02462382 describes a study currently listed as completed, categorized as Phase 4. The registered enrollment target is 51 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Orlando Health, which has 21 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Full-thickness Rotator Cuff Tear appearing as the primary indexed condition, and to 3 interventions - of which Saline is the first listed.
NCT02462382 reports 1 study location spanning 1 distinct geographic area - top geographies include Florida.
Frequently Asked Questions
What is clinical trial NCT02462382 about?
NCT02462382 is a clinical study titled "Efficacy of Continuous Infusion Ropivacaine Interscalene Blocks". Arthroscopic rotator cuff repair is a common and painful procedure routinely performed on an outpatient basis. Postoperative pain control regimens can include narcotic pain medicine, non-steroidal anti-inflammatory medications and regional anesthesia such as an interscalene block (ISB). Regional blo...
What is the current status of trial NCT02462382?
This trial is currently completed. It is a Phase 4 study. The enrollment target is 51 participants. The study started on 2013-09-01. Estimated completion is 2016-05-20.
What conditions does trial NCT02462382 study?
This clinical trial studies the following conditions: Full-thickness Rotator Cuff Tear.
What interventions are being tested in trial NCT02462382?
The interventions under investigation include: Saline (DRUG), Ropivacaine (DRUG), Arthroscopic Rotator Cuff Repair (PROCEDURE).
Who is sponsoring clinical trial NCT02462382?
This trial is sponsored by Orlando Health, which has 21 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT02462382 being conducted?
This trial has 1 study location across Florida. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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