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NCT02730728 · ClinicalTrials.gov registry record · NA
Single Shot vs 24hr vs 48hr Continuous Adductor Canal Block After TKA
A NA study of Osteoarthritis and Total Knee Arthroplasty, sponsored by University of Pennsylvania.
- Completed
- Registry status
- NA
- Development phase
- 159
- Enrollment target
- 1
- Study location
NCT02730728 is a NA study of Osteoarthritis and Total Knee Arthroplasty that has completed, run by University of Pennsylvania. The registered enrollment target is 159 participants, below the 817-participant average among 135 other Osteoarthritis trials with a reported enrollment target (81% lower). The trial reports 1 study location across 1 state.
The verdict
NCT02730728, a NA study of Osteoarthritis and Total Knee Arthroplasty, has completed, sponsored by University of Pennsylvania.
- COMPLETED
- Registry status
- NA
- Development phase
- 159 participants
- Enrollment target
- 1
- Study location
Study Summary
The purpose of this study is to compare a single shot block, 24 hours, and 48 hour continuous catheter nerve block done via the adductor canal method in adult patients who have under gone total knee arthroplasty. Visual analogue scores, opioid consumption, time to up and go, ambulation, manual muscle tests, and Tinetti scores up to 72 hours post operatively will be used for comparison.
Conditions Studied
Interventions
- DRUG 20ml bolus of 0.5% ropivicaine
- DRUG 0.2% Ropivicaine at 8 milliliter/hour
- DRUG 5ml bolus of 0.5% ropivicaine
Study Locations (1)
Pennsylvania
- University of Pennsylvania - Philadelphia
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 159 participants |
| Start Date | 2015-11-01 |
| Est. Completion | 2017-01-01 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT02730728
The ClinicalTrials.gov registry entry for NCT02730728 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 159 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 817-participant average among 135 other Osteoarthritis trials with a reported enrollment target (81% lower). The listed sponsor is University of Pennsylvania, which has 1,423 total studies on file at ClinicalTrials.gov.
The record links to 3 conditions, with Osteoarthritis appearing as the primary indexed condition, and to 3 interventions - of which 20ml bolus of 0.5% ropivicaine is the first listed.
NCT02730728 reports 1 study location spanning 1 distinct geographic area - top geographies include Pennsylvania.
Frequently Asked Questions
What is clinical trial NCT02730728 about?
NCT02730728 is a clinical study titled "Single Shot vs 24hr vs 48hr Continuous Adductor Canal Block After TKA". The purpose of this study is to compare a single shot block, 24 hours, and 48 hour continuous catheter nerve block done via the adductor canal method in adult patients who have under gone total knee arthroplasty. Visual analogue scores, opioid consumption, time to up and go, ambulation, manual muscl...
What is the current status of trial NCT02730728?
This trial is currently completed. It is a NA study. The enrollment target is 159 participants. The study started on 2015-11-01. Estimated completion is 2017-01-01.
What conditions does trial NCT02730728 study?
This clinical trial studies the following conditions: Osteoarthritis, Total Knee Arthroplasty, Post Operative Pain Control.
What interventions are being tested in trial NCT02730728?
The interventions under investigation include: 20ml bolus of 0.5% ropivicaine (DRUG), 0.2% Ropivicaine at 8 milliliter/hour (DRUG), 5ml bolus of 0.5% ropivicaine (DRUG).
Who is sponsoring clinical trial NCT02730728?
This trial is sponsored by University of Pennsylvania, which has 1,423 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT02730728 being conducted?
This trial has 1 study location across Pennsylvania. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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