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COMPLETED NA

Multicenter Continuous Peripheral Nerve Block Surveillance Study

NCT00653133 · View on ClinicalTrials.gov ↗

Study Summary

This two tiered study is a multi-center, open label, surveillance study of the use of continuous nerve blocks with the ON-Q® C-bloc and either nerve stimulator or ultrasound guided continuous nerve block techniques. This study was developed to investigate specific aspects of complication rates related to continuous nerve block techniques in patients undergoing orthopedic surgical procedures.

Conditions Studied

Interventions

  • DEVICE Ultrasound imaging
  • DEVICE Peripheral nerve stimulator

Study Locations (16)

Texas

  • Memorial Herman Hospital — Houston
  • Titus Regional Medical Center — Mount Pleasant

Arizona

  • Arizona Joint and Spine — Chandler

California

  • Santa Clara Valley Medical Center — San Jose

Colorado

  • Avista Adventist Hospital — Louisville

Georgia

  • Kennestone Hospital — Atlanta

Kentucky

  • The Medical Center of Bowling Green — Bowling Green

Massachusetts

  • Caritas Good Samaritan — Stoughton

Mississippi

  • Wesley Medical Center — Hattiesburg

Trial Details

FieldValue
Enrollment Target 1,821 participants
Start Date 2007-05
Est. Completion 2009-03
Phase NA

Sponsor

Halyard Health

3 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT00653133

The ClinicalTrials.gov registry entry for NCT00653133 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 1,821 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Halyard Health, which has 3 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 Postoperative Pain appearing as the primary indexed condition, and to 2 interventions — of which Ultrasound imaging 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: NCT00653133 reports 16 study locations spanning 15 distinct geographic areas — top geographies include Texas, Arizona, California. 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 NCT00653133 about?

NCT00653133 is a clinical study titled "Multicenter Continuous Peripheral Nerve Block Surveillance Study". This two tiered study is a multi-center, open label, surveillance study of the use of continuous nerve blocks with the ON-Q® C-bloc and either nerve stimulator or ultrasound guided continuous nerve block techniques. This study was developed to investigate specific aspects of complication rates relat...

What is the current status of trial NCT00653133?

This trial is currently completed. It is a NA study. The enrollment target is 1,821 participants. The study started on 2007-05. Estimated completion is 2009-03.

What conditions does trial NCT00653133 study?

This clinical trial studies the following conditions: Postoperative Pain. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT00653133?

The interventions under investigation include: Ultrasound imaging (DEVICE), Peripheral nerve stimulator (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT00653133?

This trial is sponsored by Halyard Health, which has 3 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT00653133 being conducted?

This trial has 16 study locations across Arizona, California, Colorado, Georgia, Kentucky. 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