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NCT01385449 · ClinicalTrials.gov registry record · NA
Prospective Evaluation of Interscalene Nerve Catheters vs. Single Injection Blocks
A NA study, sponsored by University of Wisconsin, Madison.
- Terminated
- Registry status
- NA
- Development phase
- 73
- Enrollment target
NCT01385449 is a NA study that was terminated before completion, run by University of Wisconsin, Madison. The registered enrollment target is 73 participants.
The verdict
NCT01385449, a NA study, was terminated before completion, sponsored by University of Wisconsin, Madison.
- TERMINATED
- Registry status
- NA
- Development phase
- 73 participants
- Enrollment target
Study Summary
The primary hypothesis is that those patients who choose an interscalene catheter will have less pain postoperatively than those with single injection blocks. Secondary hypotheses examine physical therapy outcomes and incidence of parasthesia or pain following surgery for up to 3 months.
Interventions
- PROCEDURE interscalene catheter
- PROCEDURE interscalene block
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 73 participants |
| Start Date | 2011-06 |
| Est. Completion | 2016-02 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01385449
The ClinicalTrials.gov registry entry for NCT01385449 describes a study currently listed as terminated, categorized as NA. The registered enrollment target is 73 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Wisconsin, Madison, which has 1,039 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which interscalene catheter is the first listed.
NCT01385449 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT01385449 about?
NCT01385449 is a clinical study titled "Prospective Evaluation of Interscalene Nerve Catheters vs. Single Injection Blocks". The primary hypothesis is that those patients who choose an interscalene catheter will have less pain postoperatively than those with single injection blocks. Secondary hypotheses examine physical therapy outcomes and incidence of parasthesia or pain following surgery for up to 3 months.
What is the current status of trial NCT01385449?
This trial is currently terminated. It is a NA study. The enrollment target is 73 participants. The study started on 2011-06. Estimated completion is 2016-02.
What interventions are being tested in trial NCT01385449?
The interventions under investigation include: interscalene catheter (PROCEDURE), interscalene block (PROCEDURE).
Who is sponsoring clinical trial NCT01385449?
This trial is sponsored by University of Wisconsin, Madison, which has 1,039 total clinical trials registered on ClinicalTrials.gov.
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