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OpenTrials
Completed

NCT Number: NCT07748143

To Evaluate the Impact of MRSA Nasal Screen Implementation.

To evaluate the impact of MRSA nasal screen implementation on duration of therapy and cost associated with vancomycin use.

Completed

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Key information

Conditions

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Methodist Dallas Medical Center- Clinical Research Institute

Dallas, Texas, 75203, United States

About this study

Routine blood and sputum cultures are often obtained inpatient for critically ill pneumonia patients. These tests, however, tend to have a high yield of false positives, leading to an increase in the use of broad spectrum antibiotics, specifically vancomycin. The Methicillin-resistant Staphylococcus aureus(MRSA) nasal screen is an antimicrobial stewardship tool that can be used to guide the treatment of community-acquired, hospital-acquired and ventilator-associated pneumonia. Due to its strong negative predictive value; a negative result can accurately indicate the absence of an MRSA infection in 96% of cases. Long-term treatment with vancomycin in patients with pneumonia is nephrotoxic and not always warranted. The implementation of an MRSA nasal screen in all patients with pneumonia treated with vancomycin has the potential to reduce vancomycin duration of therapy, decrease the risk of adverse effects and decrease the cost associated with vancomycin use.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age > 18 years
  • Diagnosis of pneumonia
  • Admission inpatient to Methodist Richardson Medical Center
  • Treatment with vancomycin empirically

Exclusion criteria

  • Age ≤ 18 years
  • Patients with other confirmed gram positive infections

Treatment and study plan

Duration of therapy

Other

The final data will then be compared to determine if the duration of therapy and cost after implementation of the MRSA nasal screen if significantly different from before the implementation of the MRSA nasal screen.

Direct cost

Other

Direct costs of vancomycin for each treatment arm (in US dollars).

Pharmacokinectic Monitoring

Other

Number of vancomycin levels drawn for pharmacokinetic monitoring.

Hospital stay

Other

Length of hospital stay in days

Primary outcomes

  1. Duration of therapy

    Time frame: 1 year

    To analyze duration of vancomycin in days.

Sponsors and collaborators

Lead sponsor

Methodist Health System

Other

Registry information

Official study title

The Effect of MRSA Nasal Screen Implementation on Duration of Therapy and Cost Associated With Vancomycin Use.

Important dates

Study start
2019
Primary completion
2026
Study completion
2026
First posted
Aug 5, 2026
Registry last updated
Aug 5, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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