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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: Completed NA study, sponsored by University of Chicago.
NCT02121392 is a NA study that has completed, run by University of Chicago. The registered enrollment target is 165 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (88% lower). According to ClinicalTrials.gov, the official US trial registry.
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 |
What the finished NCT02121392 record still lists
NCT02121392 is an interventional study that assigns participants to a tested intervention. The registered 165 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (88% lower).
The record links to 0 conditions, and to 3 interventions - of which Bupivacaine is the first listed.
NCT02121392 does not publish any study locations in the registry export this page uses.
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.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT02121392's enrollment target sits among peer trials
165 626th of 2000 higher than 1,375 of 2,000 other NA trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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