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NCT02121392 · ClinicalTrials.gov registry record · NA
Epidural Catheter With or Without Adductor Canal Nerve Block for Postoperative Analgesia Following Total Knee Arthroplasty
A NA study, sponsored by University of Chicago.
- Completed
- Registry status
- NA
- Development phase
- 165
- Enrollment target
NCT02121392 is a NA study that has completed, run by University of Chicago. The registered enrollment target is 165 participants.
The verdict
NCT02121392, a NA study, has completed, sponsored by University of Chicago.
- COMPLETED
- Registry status
- NA
- Development phase
- 165 participants
- Enrollment target
Study Summary
The purpose of this study is to further investigate the efficacy of adductor canal nerve blocks for pain management after total knee replacement. Specifically we are studying adductor canal nerve blocks in conjunction with epidural anesthesia, which is a combination that has not been extensively researched before. Our question is whether combining these modalities will enhance patient satisfaction after surgery and accelerate patients' readiness to discharge.
Interventions
- DRUG Bupivacaine
- DEVICE Adductor Canal Nerve Block Catheter
- DEVICE Adductor Canal Nerve Block Sham Catheter
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 165 participants |
| Start Date | 2014-10 |
| Est. Completion | 2017-01 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT02121392
The ClinicalTrials.gov registry entry for NCT02121392 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 165 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Chicago, which has 796 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 3 interventions - of which Bupivacaine is the first listed.
NCT02121392 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT02121392 about?
NCT02121392 is a clinical study titled "Epidural Catheter With or Without Adductor Canal Nerve Block for Postoperative Analgesia Following Total Knee Arthroplasty". The purpose of this study is to further investigate the efficacy of adductor canal nerve blocks for pain management after total knee replacement. Specifically we are studying adductor canal nerve blocks in conjunction with epidural anesthesia, which is a combination that has not been extensively res...
What is the current status of trial NCT02121392?
This trial is currently completed. It is a NA study. The enrollment target is 165 participants. The study started on 2014-10. Estimated completion is 2017-01.
What interventions are being tested in trial NCT02121392?
The interventions under investigation include: Bupivacaine (DRUG), Adductor Canal Nerve Block Catheter (DEVICE), Adductor Canal Nerve Block Sham Catheter (DEVICE).
Who is sponsoring clinical trial NCT02121392?
This trial is sponsored by University of Chicago, which has 796 total clinical trials registered on ClinicalTrials.gov.
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