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Study to Evaluate ACB Versus FNB Early Postoperative Period Functional Outcomes After TKA
NCT02218814 · View on ClinicalTrials.gov ↗
Study Summary
The purpose of this study is to determine if patients undergoing a Total Knee Arthroplasty who receive a single shot Adductor Canal nerve block and local infiltration will have improved functional outcomes compared to individuals who receive a femoral nerve block and local infiltration during the first 24 hours post surgery.
Conditions Studied
Interventions
- PROCEDURE Adductor Canal Block, Bupivacaine
- PROCEDURE Femoral Nerve Block, Bupivacaine
Study Locations (1)
Illinois
- Presence Saint Joseph Medical Center — Joliet
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 106 participants |
| Start Date | 2014-08 |
| Est. Completion | 2016-01 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT02218814
The ClinicalTrials.gov registry entry for NCT02218814 describes a study currently listed as completed. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 106 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is George Macrinici, which has 1 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 2 conditions, with Arthroplasty, Replacement, Knee appearing as the primary indexed condition, and to 2 interventions — of which Adductor Canal Block, Bupivacaine is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT02218814 reports 1 study location spanning 1 distinct geographic area — top geographies include Illinois. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT02218814 about?
NCT02218814 is a clinical study titled "Study to Evaluate ACB Versus FNB Early Postoperative Period Functional Outcomes After TKA". The purpose of this study is to determine if patients undergoing a Total Knee Arthroplasty who receive a single shot Adductor Canal nerve block and local infiltration will have improved functional outcomes compared to individuals who receive a femoral nerve block and local infiltration during the fi...
What is the current status of trial NCT02218814?
This trial is currently completed. It is a NA study. The enrollment target is 106 participants. The study started on 2014-08. Estimated completion is 2016-01.
What conditions does trial NCT02218814 study?
This clinical trial studies the following conditions: Arthroplasty, Replacement, Knee, Nerve Block. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT02218814?
The interventions under investigation include: Adductor Canal Block, Bupivacaine (PROCEDURE), Femoral Nerve Block, Bupivacaine (PROCEDURE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT02218814?
This trial is sponsored by George Macrinici, which has 1 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT02218814 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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