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NCT01763814 · ClinicalTrials.gov registry record · NA
Three Different Approaches for Ultrasound Guided Femoral Nerve Block for Patients Undergoing Total Knee Arthroplasty
A NA study of Knee Arthroplasty, sponsored by Chicago Anesthesia Pain Specialists.
- Completed
- Registry status
- NA
- Development phase
- 108
- Enrollment target
- 1
- Study location
NCT01763814: Completed NA study of Knee Arthroplasty, sponsored by Chicago Anesthesia Pain Specialists.
NCT01763814 is a NA study of Knee Arthroplasty that has completed, run by Chicago Anesthesia Pain Specialists. The registered enrollment target is 108 participants, below the 715-participant average among 5 other Knee Arthroplasty trials with a reported enrollment target (85% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01763814, a NA study of Knee Arthroplasty, has completed, sponsored by Chicago Anesthesia Pain Specialists.
- COMPLETED
- Registry status
- NA
- Development phase
- 108 participants
- Enrollment target
- 1
- Study location
Study Summary
Patients scheduled to have a surgery for Total Knee Arthroplasty will be assigned to one of three groups, each group will use a different approach using the ultrasound to guide the femoral nerve block as part of their treatment for controlling pain post-operatively.
Primary Outcome
At the conclusion of the surgery time 0, at 15, 30, and 45 minutes, at 1, 12, 24, 48 hours, and day 3, 7, 14, and 30 after the surgery.
Conditions Studied
Interventions
- PROCEDURE Femoral nerve block
- PROCEDURE Femoral nerve block non stimulating catheter
- PROCEDURE Femoral nerve block stimulating catheter
Study Locations (1)
Illinois
- Chicago Anesthesia Pain Specialists - Chicago
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 108 participants |
| Start Date | 2011-12 |
| Est. Completion | 2019-04 |
| Phase | NA |
What the finished NCT01763814 record still lists
NCT01763814 is an interventional study that assigns participants to a tested intervention. The registered 108 participants enrollment target is mid-sized for trials with a published cap, below the 715-participant average among 5 other Knee Arthroplasty trials with a reported enrollment target (85% lower).
The record links to 1 condition, with Knee Arthroplasty appearing as the primary indexed condition, and to 3 interventions - of which Femoral nerve block is the first listed.
NCT01763814 reports a single indexed study location in Illinois.
Frequently Asked Questions
What is clinical trial NCT01763814 about?
NCT01763814 is a clinical study titled "Three Different Approaches for Ultrasound Guided Femoral Nerve Block for Patients Undergoing Total Knee Arthroplasty". Patients scheduled to have a surgery for Total Knee Arthroplasty will be assigned to one of three groups, each group will use a different approach using the ultrasound to guide the femoral nerve block as part of their treatment for controlling pain post-operatively.
What is the current status of trial NCT01763814?
This trial is currently completed. It is a NA study. The enrollment target is 108 participants. The study started on 2011-12. Estimated completion is 2019-04.
What conditions does trial NCT01763814 study?
This clinical trial studies the following conditions: Knee Arthroplasty.
What interventions are being tested in trial NCT01763814?
The interventions under investigation include: Femoral nerve block (PROCEDURE), Femoral nerve block non stimulating catheter (PROCEDURE), Femoral nerve block stimulating catheter (PROCEDURE).
Who is sponsoring clinical trial NCT01763814?
This trial is sponsored by Chicago Anesthesia Pain Specialists, which has 2 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT01763814 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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