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NCT02415465 · ClinicalTrials.gov registry record · NA
Continuous Adductor Canal Block (CACB) vs. Combined Spinal Epidural (CSE) in Total Knee Arthroplasty
A NA study of Arthroplasty, sponsored by Rush University Medical Center.
- Completed
- Registry status
- NA
- Development phase
- 157
- Enrollment target
- 1
- Study location
NCT02415465: Completed NA study of Arthroplasty, sponsored by Rush University Medical Center.
NCT02415465 is a NA study of Arthroplasty that has completed, run by Rush University Medical Center. The registered enrollment target is 157 participants, below the 210-participant average among 5 other Arthroplasty trials with a reported enrollment target (25% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT02415465, a NA study of Arthroplasty, has completed, sponsored by Rush University Medical Center.
- COMPLETED
- Registry status
- NA
- Development phase
- 157 participants
- Enrollment target
- 1
- Study location
Study Summary
Purpose: Compare continuous adductor canal block (CACB) to Combined Spinal Epidural (CSE) for total knee arthroplasty in terms of mobility, post-operative pain, and analgesic use. Hypothesis: CACB will provide better mobility than CSE post operatively.
Primary Outcome
Patient ambulation distance will be measured daily after surgery until discharge from hospital
Conditions Studied
Interventions
- PROCEDURE Epidural
- PROCEDURE Continuous Adductor Canal Block
- PROCEDURE General
- PROCEDURE Spinal
Study Locations (1)
Illinois
- Rush University Medical Center - Chicago
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 157 participants |
| Start Date | 2015-01 |
| Est. Completion | 2016-03 |
| Phase | NA |
What the finished NCT02415465 record still lists
NCT02415465 is an interventional study that assigns participants to a tested intervention. The registered 157 participants enrollment target is mid-sized for trials with a published cap, below the 210-participant average among 5 other Arthroplasty trials with a reported enrollment target (25% lower).
The record links to 1 condition, with Arthroplasty appearing as the primary indexed condition, and to 4 interventions - of which Epidural is the first listed.
NCT02415465 reports a single indexed study location in Illinois.
Frequently Asked Questions
What is clinical trial NCT02415465 about?
NCT02415465 is a clinical study titled "Continuous Adductor Canal Block (CACB) vs. Combined Spinal Epidural (CSE) in Total Knee Arthroplasty". Purpose: Compare continuous adductor canal block (CACB) to Combined Spinal Epidural (CSE) for total knee arthroplasty in terms of mobility, post-operative pain, and analgesic use. Hypothesis: CACB will provide better mobility than CSE post operatively.
What is the current status of trial NCT02415465?
This trial is currently completed. It is a NA study. The enrollment target is 157 participants. The study started on 2015-01. Estimated completion is 2016-03.
What conditions does trial NCT02415465 study?
This clinical trial studies the following conditions: Arthroplasty.
What interventions are being tested in trial NCT02415465?
The interventions under investigation include: Epidural (PROCEDURE), Continuous Adductor Canal Block (PROCEDURE), General (PROCEDURE), Spinal (PROCEDURE).
Who is sponsoring clinical trial NCT02415465?
This trial is sponsored by Rush University Medical Center, which has 320 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT02415465 being conducted?
This trial has 1 study location across Illinois. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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