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NCT01409278 · ClinicalTrials.gov registry record · NA
Local Anesthetic Infiltration and Infusion for Pain Control After Hip Replacement
A NA study, sponsored by Trinity Health Of New England.
- Completed
- Registry status
- NA
- Development phase
- 105
- Enrollment target
NCT01409278 is a NA study that has completed, run by Trinity Health Of New England. The registered enrollment target is 105 participants.
The verdict
NCT01409278, a NA study, has completed, sponsored by Trinity Health Of New England.
- COMPLETED
- Registry status
- NA
- Development phase
- 105 participants
- Enrollment target
Study Summary
The purpose of this study is to examine three different ways to control pain after hip replacement: 1. One time injection of ropivacaine before wound closure 2. One time injection of ropivacaine before wound closure plus slow release of ropivacaine via catheter for 48 hours 3. Standard practice of patient controlled pump
Interventions
- PROCEDURE Normal Saline
- PROCEDURE Ropivacaine infiltration and saline infusion.
- PROCEDURE Ropivacaine infiltration and infusion.
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 105 participants |
| Start Date | 2009-08 |
| Est. Completion | 2011-06 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01409278
The ClinicalTrials.gov registry entry for NCT01409278 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 105 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Trinity Health Of New England, which has 20 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 3 interventions - of which Normal Saline is the first listed.
NCT01409278 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT01409278 about?
NCT01409278 is a clinical study titled "Local Anesthetic Infiltration and Infusion for Pain Control After Hip Replacement". The purpose of this study is to examine three different ways to control pain after hip replacement: 1. One time injection of ropivacaine before wound closure 2. One time injection of ropivacaine before wound closure plus slow release of ropivacaine via catheter for 48 hours 3. Standard practice of ...
What is the current status of trial NCT01409278?
This trial is currently completed. It is a NA study. The enrollment target is 105 participants. The study started on 2009-08. Estimated completion is 2011-06.
What interventions are being tested in trial NCT01409278?
The interventions under investigation include: Normal Saline (PROCEDURE), Ropivacaine infiltration and saline infusion. (PROCEDURE), Ropivacaine infiltration and infusion. (PROCEDURE).
Who is sponsoring clinical trial NCT01409278?
This trial is sponsored by Trinity Health Of New England, which has 20 total clinical trials registered on ClinicalTrials.gov.
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