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NCT01126593 · ClinicalTrials.gov registry record · NA
Post-Op Rotator Cuff Pain Study With Subacromial Bupivacaine Infusion
A NA study, sponsored by Orlando Health.
- Completed
- Registry status
- NA
- Development phase
- 96
- Enrollment target
NCT01126593 is a NA study that has completed, run by Orlando Health. The registered enrollment target is 96 participants.
The verdict
NCT01126593, a NA study, has completed, sponsored by Orlando Health.
- COMPLETED
- Registry status
- NA
- Development phase
- 96 participants
- Enrollment target
Study Summary
Subacromial pain catheters have been used with uncertain efficacy for many years after rotator cuff repair to aid in postoperative pain control. Our null hypothesis is that postoperative subacromial continuous infusion bupivacaine catheters will provide no pain control benefits over placebo infusions or no catheter use.
Interventions
- DRUG Normal Saline
- DRUG 0.5% bupivacaine
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 96 participants |
| Start Date | 2008-12 |
| Est. Completion | 2010-02 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01126593
The ClinicalTrials.gov registry entry for NCT01126593 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 96 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 0 conditions, and to 2 interventions - of which Normal Saline is the first listed.
NCT01126593 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT01126593 about?
NCT01126593 is a clinical study titled "Post-Op Rotator Cuff Pain Study With Subacromial Bupivacaine Infusion". Subacromial pain catheters have been used with uncertain efficacy for many years after rotator cuff repair to aid in postoperative pain control. Our null hypothesis is that postoperative subacromial continuous infusion bupivacaine catheters will provide no pain control benefits over placebo infusion...
What is the current status of trial NCT01126593?
This trial is currently completed. It is a NA study. The enrollment target is 96 participants. The study started on 2008-12. Estimated completion is 2010-02.
What interventions are being tested in trial NCT01126593?
The interventions under investigation include: Normal Saline (DRUG), 0.5% bupivacaine (DRUG).
Who is sponsoring clinical trial NCT01126593?
This trial is sponsored by Orlando Health, which has 21 total clinical trials registered on ClinicalTrials.gov.
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