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COMPLETED NA

Three Different Approaches for Ultrasound Guided Femoral Nerve Block for Patients Undergoing Total Knee Arthroplasty

NCT01763814 · View on ClinicalTrials.gov ↗

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.

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

FieldValue
Enrollment Target 108 participants
Start Date 2011-12
Est. Completion 2019-04
Phase NA

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT01763814

The ClinicalTrials.gov registry entry for NCT01763814 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 108 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Chicago Anesthesia Pain Specialists, 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 1 condition, with Knee Arthroplasty appearing as the primary indexed condition, and to 3 interventions — of which Femoral nerve block 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: NCT01763814 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 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. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

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). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT01763814?

This trial is sponsored by Chicago Anesthesia Pain Specialists, 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 NCT01763814 being conducted?

This trial has 1 study location across Illinois. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial