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Clinical trialNCT01349192TerminatedPhase 2Interventional

Early Methicillin-resistant Staphylococcus Aureus (MRSA) Therapy in Cystic Fibrosis (CF)

SponsorUniversity of North Carolina, Chapel HillEnrollment47Cystic FibrosisMethicillin-resistant Staphylococcus Aureus
View the registry record on ClinicalTrials.gov

Summary

The lay summary the sponsor registered on ClinicalTrials.gov.

Purpose: There has been a recent, rapid increase in prevalence of Methicillin-resistant Staphylococcus aureus (MRSA) among patients with Cystic Fibrosis (22% across US CF centers in 2009). Some epidemiologic studies suggest possible worse outcomes, a recent analyses showing this with chronic but not intermittent MRSA. Given the chronic difficult to treat lung infections in CF it is unclear how the onset of MRSA should be approached. This randomized, controlled, interventional study seeks to determine if an early eradication protocol is effective for eradication of MRSA and will provide an opportunity to obtain data regarding early clinical impact of new isolation of MRSA. Participants: Cystic fibrosis patients with new isolation of MRSA from their respiratory culture on a routine clinic visit. Procedures (methods): Randomized, open-label, multi-center study comparing use of an eradication protocol to an observational group who receives the current standard of care i.e. treatment for MRSA only with pulmonary exacerbations.

Investigators

The overall officials registered on this study. Names that resolve to a FindMyKOL profile link to it; the rest are shown as registered.

A profile link is shown only when the registered name resolves to a person record with a confident, namesake-checked match; ambiguous names stay unlinked.

Sites

13 registered facilities, with the per-site recruitment status where the registry publishes one. ClinicalTrials.gov does not publish per-site enrollment counts.

United States
  • the Children'S Hospital-University of Birmingham

    Birmingham, Alabama, United States

  • the Children'S Hospital

    Aurora, Colorado, United States

  • University of Florida

    Gainesville, Florida, United States

  • University of Michigan Health System

    Ann Arbor, Michigan, United States

  • Children'S Hospitals and Clinics of Minnesota Minneapolis

    Minneapolis, Minnesota, United States

  • St. Louis Children'S Hospital

    St Louis, Missouri, United States

  • N.C Memorial Hospital and N.C Children'S Hospital

    Chapel Hill, North Carolina, United States

  • Cff Care Center & Pediatric Program Cincinnati Children'S Hospital Medical Center

    Cincinnati, Ohio, United States

  • University of Texas Southwestern Medical Center

    Dallas, Texas, United States

  • Cook Children'S Medical Center

    Fort Worth, Texas, United States

  • Baylor College of Medicine

    Houston, Texas, United States

  • Seattle Children'S

    Seattle, Washington, United States

  • University of Washington Medical Center

    Seattle, Washington, United States

Site investigator names are published by ClinicalTrials.gov only while a study recruits, so completed studies list sites without them.

Drugs studied

The drug and biological interventions registered on this study, normalized to their RxNorm ingredient where possible.

2% Chlorhexidine solution wipesMinocycline →Mupirocin →Rifampin →Trimethoprim →Chlorhexidine gluconate oral rinse
Linked drugs open the directory filtered to KOLs working with them.clinicaltrials.gov ↗

Registration & key dates

Registry attributes as recorded on the ClinicalTrials.gov study record.

Start
30 Apr 2011
Primary completion
31 Jan 2015
Completion
31 May 2015
Last update posted
15 May 2017
Registered enrollment
47
Registry id
NCT01349192

Source: ClinicalTrials.gov, via the CTTI AACT database, data as of 24 Aug 2026. Registry facts are shown as registered by the study sponsor; FindMyKOL does not interpret them.