Early Methicillin-resistant Staphylococcus Aureus (MRSA) Therapy in Cystic Fibrosis (CF) (STAR-Too)
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Purpose
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.
| Condition | Intervention | Phase |
|---|---|---|
|
Cystic Fibrosis Methicillin-resistant Staphylococcus Aureus |
Drug: Rifampin Drug: Trimethoprim/Sulfamethoxazole Drug: Minocycline Drug: Mupirocin Drug: chlorhexidine gluconate oral rinse Drug: 2% Chlorhexidine solution wipes Behavioral: Environmental Decontamination |
Phase 2 |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Safety/Efficacy Study Intervention Model: Parallel Assignment Masking: Open Label Primary Purpose: Treatment |
| Official Title: | Early MRSA Therapy in CF - Culture Based vs. Observant Therapy (Treat or Observe) (Star-TOO - STaph Aureus Resistance - Treat or Observe) |
- Microbiology [ Time Frame: Day 28 ] [ Designated as safety issue: No ]Proportion of subjects in each arm with MRSA negative respiratory cultures at day 28.
- Antibiotic Use [ Time Frame: 6 months ] [ Designated as safety issue: No ]proportion of subjects treated with oral, inhaled, and IV antibiotics over the 6 month study and number of days of use.
- Exacerbation [ Time Frame: 6 months ] [ Designated as safety issue: No ]Proportion of subjects with a protocol defined pulmonary exacerbation between baseline and day 28 who are treated with antibiotics active against MRSA.
| Estimated Enrollment: | 80 |
| Study Start Date: | April 2011 |
| Estimated Study Completion Date: | December 2013 |
| Estimated Primary Completion Date: | July 2013 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
Experimental: Treatment
Subjects are treated with two oral antibiotics, topical antibiotics, and are instructed to use environmental decontamination techniques.
|
Drug: Rifampin
Adult Dose: 300mg twice daily for 14 days. Pediatric Dose: <40kg : 15mg/kg daily for 14 days divided every 12 hours.
Other Name: Rifadin, Rimactane
Drug: Trimethoprim/Sulfamethoxazole
Adult Dose: 320/1600 orally twice daily for 14 days. Pediatric Dose: <40 kg : 8mg/kg trimethoprim / 40 mg/kg sulfamethoxazole twice a day for 14 days.
Other Name: Bactrim, Septra
Drug: Minocycline
only subjects greater or equal to 8 years of age, who are not able to tolerate TMP/SMX or whose screening MRSA is resistant to TMP/SMX should be prescribed minocycline. Adult dose: 100 mg orally twice daily for 14 days Pediatric dose: < 50 kg : 2mg/kg orally twice daily for 14 days not to exceed 200mg per day. Other Name: Cleeravue-M, Dynacin, Minocin, Myrac, Solodyn, Vectrin
Drug: Mupirocin
1 gram 2% nasal ointment generously applied to each nostril using a cotton swab twice daily for 14 days.
Other Name: Bactroban, Centany
Drug: chlorhexidine gluconate oral rinse
for subjects able to swish without swallowing. 0.12% chlorhexidine gluconate oral rinse twice daily for 14 days.
Drug: 2% Chlorhexidine solution wipes
whole body wash solution wipes once daily for first 5 days.
Behavioral: Environmental Decontamination
wipe down high touch surfaces and medical equipment with surface disinfecting wipes daily for the first 21 days. wash all linens and towels in hot water once weekly for three weeks. Other Name: Sani-Cloth Plus
|
|
No Intervention: Observational
Subjects are tracked and not treated for their MRSA. If the subject reaches a protocol defined exacerbation within the first 28 days then they will be treated per choice of their primary Pulmonologist.
|
Eligibility| Ages Eligible for Study: | 4 Years to 45 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- Male or female ≥ 4 and ≤ 45 years of age at the Screening Visit.
Documentation of a CF diagnosis as evidenced by one or more clinical features consistent with the CF phenotype and one or more of the following criteria:
- sweat chloride ≥ 60 mEq/liter by quantitative pilocarpine iontophoresis test (QPIT)
- two well-characterized mutations in the cystic fibrosis transmembrane conductive regulator (CFTR) gene
- Abnormal nasal potential difference (change in NPD in response to a low chloride solution and isoproteronol of less than -5 mV)
First OR early repeat MRSA colonization defined as:
- First MRSA colonization: first documented isolation of MRSA from respiratory tract occurred ≤ 6 months prior to screening
- OR Early repeat MRSA colonization:
MRSA was previously isolated from the respiratory tract (≤ 2 times), but this was followed by at least 1 year of documented negative cultures for MRSA as noted below:
-- At least 2 cultures performed at least 3 months apart to document 1 year of culture negativity. Each of these cultures should be documented to have been collected at least 1 week after end of any antibiotic prescription with MRSA activity.
Patient again recently positive for MRSA from the respiratory tract (within 6 months prior to screening)
- Clinically stable with no significant changes in health status within the 14 days prior to screening
- Written informed consent (and assent when applicable) obtained from subject or subject's legal representative and ability for subject to comply with the requirements of the study
A repeat culture from the respiratory tract is obtained at screening but does not have to be positive to be able to enter the study.
Exclusion Criteria:
- Received antibiotics with activity against MRSA within 28 days prior to screening (see study manual for list of antibiotics)
- Use of an investigational agent within 28 days prior to screening
- For subjects ≥ 6 years of age: FEV1 at screening < 30% of predicted for age based on the Wang (males < 18 years, females < 16 years) or Hankinson (males ≥ 18 years, females ≥ 16 years) standardized equations
- MRSA from the screening culture resistant to rifampin OR resistant to both TMP/SMX and minocycline
- History of intolerance to oral rifampin, or topical chlorhexidine or mupirocin
- History of intolerance to both TMP/SMX and minocycline
- < 8 years of age and either allergic or intolerant to TMP/SMX or screening MRSA resistant to TMP/SMX
- ≥ 8 years of age and allergic or intolerant to TMP/SMX and screening MRSA resistant to minocycline
- ≥ 8 years of age and allergic or intolerant to minocycline and screening MRSA resistant to TMP/SMX
- For females of child bearing potential: pregnant, breastfeeding, or unwilling to use barrier contraception through Day 15 of the study
- Abnormal renal function at Screening, defined as estimated creatinine clearance <50 mL/min using the Cockcroft-Gault equation
- Abnormal liver function at the time of screening, defined as ≥2x upper limit of normal (ULN), of serum aspartate transaminase (AST) or serum alanine transaminase (ALT)
- History of solid organ or hematological transplantation
- Presence of a condition or abnormality that in the opinion of the Investigator would compromise the safety of the patient or the quality of the data.
Contacts and Locations| Contact: Jill Van Dalfsen | 206-884-7509 | jill.vandalfsen@seattlechildrens.org |
| Contact: Marianne S Muhlebach, MD | 919-966-1055 | Marianne_Muhlebach@med.unc.edu |
| United States, Alabama | |
| The Children's Hospital-University of Birmingham | Recruiting |
| Birmingham, Alabama, United States, 35233 | |
| Contact: Ginger Reeves 205-939-5970 greeves@peds.uab.edu | |
| Principal Investigator: Wynton Hoover | |
| United States, Colorado | |
| The Children's Hospital | Recruiting |
| Aurora, Colorado, United States, 80045 | |
| Contact: Meg Anthony 720-777-2945 anthony.meg@tchden.org | |
| Principal Investigator: Edith Zemanick | |
| United States, Florida | |
| University of Florida | Recruiting |
| Gainesville, Florida, United States, 32611 | |
| Contact: Dawn Baker, RN 352-273-5417 bakerdj@peds.ufl.edu | |
| Principal Investigator: Pamela Schuler, MD | |
| United States, Michigan | |
| University of Michigan Health System | Recruiting |
| Ann Arbor, Michigan, United States, 48109-5212 | |
| Contact: Marisa Linn 734-615-1372 mlinn@med.umich.edu | |
| Principal Investigator: Amy Filbrun | |
| United States, Minnesota | |
| Children's Hospitals and Clinics of Minnesota Minneapolis | Recruiting |
| Minneapolis, Minnesota, United States, 55404 | |
| Contact: Andrea Gruber, RN 612-813-6661 andrea.gruber@childrensmn.org | |
| Principal Investigator: John McNamara, MD | |
| United States, Missouri | |
| St. Louis Children's Hospital | Recruiting |
| St. Louis, Missouri, United States, 63110 | |
| Contact: Mary Boyle 314-454-4609 boyle@kids.wustl.edu | |
| Principal Investigator: Peter Michelson | |
| United States, Nebraska | |
| University of Nebraska Medical Center | Active, not recruiting |
| Omaha, Nebraska, United States, 68198-5190 | |
| United States, North Carolina | |
| N.C Memorial Hospital and N.C Children's Hospital | Recruiting |
| Chapel Hill, North Carolina, United States, 27599 | |
| Contact: Sara Bell, BS 919-966-1055 sara_bell@med.unc.edu | |
| Principal Investigator: Marianne S Muhlebach, MD | |
| United States, Ohio | |
| CFF Care Center & Pediatric Program Cincinnati Children's Hospital Medical Center | Recruiting |
| Cincinnati, Ohio, United States, 45229-3026 | |
| Contact: Duan Lorrie 513-636-7089 lorrie.duan@cchmc.org | |
| Principal Investigator: John P Clancy, MD | |
| United States, Texas | |
| University of Texas Southwestern Medical Center | Recruiting |
| Dallas, Texas, United States, 75390 | |
| Contact: Carolyne Cannon, MD 214-648-8709 | |
| Principal Investigator: Carolyn Cannon, MD | |
| Cook Children's Medical Center | Recruiting |
| Fort Worth, Texas, United States, 76104 | |
| Contact: Sara Scott 682-885-1244 Sara.Scott@CookChildrens.org | |
| Principal Investigator: James Cunningham | |
| Baylor College of Medicine | Recruiting |
| Houston, Texas, United States, 77030 | |
| Contact: Charlene Hallmark 832-822-4772 clhallma@texaschildrenshospital.org | |
| Principal Investigator: Siby Moonumakal | |
| United States, Washington | |
| University of Washington Medical Center | Recruiting |
| Seattle, Washington, United States, 98195 | |
| Contact: Alycia Wolfstone 206-685-3995 aewolf@u.washington.edu | |
| Principal Investigator: Christopher Goss, MD | |
| Seattle Children's | Recruiting |
| Seattle, Washington, United States, 98145-9807 | |
| Contact: Sharon McNamara 206-987-3921 ext 1 sharon.mcnamara@seattlechildrens.org | |
| Principal Investigator: Ronald Gibson | |
| Principal Investigator: | Marianne S Muhlebach, MD | UNC Children's Hospital |
| Principal Investigator: | Chris Goss, MD | University of Washington |
More Information
No publications provided
| Responsible Party: | Marianne Muhlebach, MD, Associate Professor, Pediatric Pulmonolgy, University of North Carolina, Chapel Hill |
| ClinicalTrials.gov Identifier: | NCT01349192 History of Changes |
| Other Study ID Numbers: | STAR-too-10K0 |
| Study First Received: | May 4, 2011 |
| Last Updated: | February 3, 2013 |
| Health Authority: | United States: Institutional Review Board |
Keywords provided by University of North Carolina, Chapel Hill:
|
MRSA Cystic Fibrosis Early Infection Treatment |
Additional relevant MeSH terms:
|
Cystic Fibrosis Fibrosis Staphylococcal Infections Pancreatic Diseases Digestive System Diseases Lung Diseases Respiratory Tract Diseases Genetic Diseases, Inborn Infant, Newborn, Diseases Pathologic Processes Gram-Positive Bacterial Infections Bacterial Infections Chlorhexidine Chlorhexidine gluconate Minocycline |
Rifampin Sulfamethoxazole Trimethoprim Mupirocin Anti-Infective Agents, Local Anti-Infective Agents Therapeutic Uses Pharmacologic Actions Disinfectants Dermatologic Agents Anti-Bacterial Agents Antibiotics, Antitubercular Antitubercular Agents Enzyme Inhibitors Molecular Mechanisms of Pharmacological Action |
ClinicalTrials.gov processed this record on June 17, 2013