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COMPLETED NA

Antimicrobial Stewardship Through MRSA Diagnosis in Emergency Department (ED) Patients With Abscesses

NCT01523899 · View on ClinicalTrials.gov ↗

Study Summary

This study expands upon pilot data for feasibility since May 2011. The study aims to evaluate the effect of rapid test availability on use of targeted spectrum antibiotics for non-MRSA abscesses in ambulatory patients in the Emergency Department (ED). The multi-institutional study will assess the feasibility of providing the GeneXpert® MRSA/SA SSTI assay to the ED and evaluate the impact of delivering the test result to clinicians in real-time on patient management decisions regarding the use of antimicrobial agents. Patients are randomized to standard culture (control arm) or to the GeneXpert® assay plus standard culture.

Conditions Studied

Interventions

  • DEVICE Xpert MRSA/SA SSTI
  • DIAGNOSTIC_TEST Standard culture

Study Locations (2)

District of Columbia

  • The George Washington University — Washington D.C.

Maryland

  • Johns Hopkins University — Baltimore

Trial Details

FieldValue
Enrollment Target 252 participants
Start Date 2011-05
Est. Completion 2015-01
Phase NA

Sponsor

George Washington University

134 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT01523899

The ClinicalTrials.gov registry entry for NCT01523899 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 252 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is George Washington University, which has 134 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 Cutaneous Abscess appearing as the primary indexed condition, and to 2 interventions — of which Xpert MRSA/SA SSTI 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: NCT01523899 reports 2 study locations spanning 2 distinct geographic areas — top geographies include District of Columbia, Maryland. 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 NCT01523899 about?

NCT01523899 is a clinical study titled "Antimicrobial Stewardship Through MRSA Diagnosis in Emergency Department (ED) Patients With Abscesses". This study expands upon pilot data for feasibility since May 2011. The study aims to evaluate the effect of rapid test availability on use of targeted spectrum antibiotics for non-MRSA abscesses in ambulatory patients in the Emergency Department (ED). The multi-institutional study will assess the fe...

What is the current status of trial NCT01523899?

This trial is currently completed. It is a NA study. The enrollment target is 252 participants. The study started on 2011-05. Estimated completion is 2015-01.

What conditions does trial NCT01523899 study?

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

What interventions are being tested in trial NCT01523899?

The interventions under investigation include: Xpert MRSA/SA SSTI (DEVICE), Standard culture (DIAGNOSTIC_TEST). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT01523899?

This trial is sponsored by George Washington University, which has 134 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT01523899 being conducted?

This trial has 2 study locations across District of Columbia, Maryland. 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