S. Aureus Oropharyngeal Colonization
Conditions
Brief summary
The problem of interest is the high rate of recurrent SSTIs in children caused by S. aureus despite the use of systemic antibiotic treatment, due to difficulties in decolonization and the prevalence of antibiotic-resistant strains such as MRSA. This problem will be studied through a randomized, double-blind, placebo-controlled clinical trial of the use of a 0.12% clorhexidine gluconate (CHG) oral rinse in decolonizing S. aureus in the oropharynx in children 5-17 years old. CHG is an excellent candidate for use in children as its safety has been widely established, and it is readily commercially available. Eligible, consented subjects will be asked to participate in a baseline study visit in which swabs of their oropharynx and nares are obtained, and they are educated on the use of either CHG oral rinse or a placebo oral rinse containing saline. The subjects will be instructed to perform the oral rinse twice daily for seven days. Two follow-up visits will occur at 7 and 28 days post-baseline, where subjects' nares and oropharynx are again swabbed in order to ascertain short- and long-term decolonization of S. aureus. This procedure will serve to 1) determine the efficacy of a CHG oral rinse in decolonization of S. aureus, 2) investigate the safety, tolerability, and compliance of oropharyngeal decolonization among children and their caregivers, and 3) determine the genetic backgrounds of strains of S. aureus associated with continued colonization.
Detailed description
Each year, children visit doctors offices and emergency rooms over 2 million times due to skin and soft tissue infections (SSTIs). These SSTIs are usually caused by a bacteria called Staphylococcus aureus (S. aureus), and can result in severe negative consequences such as hospitalization, disability, and even death. Despite treatment with antibiotics, 20-70% of children with an SSTI will develop a recurrent infection within the next year. Additionally, this treatment fails to eradicate S. aureus from children nearly 50% of the time. Of the types of S. aureus that cause these infections, antibiotic-resistant strains such as methicillin-resistant S. aureus (MRSA), which are associated with higher rates of transmission, have become increasingly more common. Thus, the problem of interest is the high rate of recurrent SSTIs in children caused by S. aureus despite the use of systemic antibiotic treatment, due to difficulties in decolonization and the prevalence of antibiotic-resistant strains such as MRSA.
Interventions
DRUGChlorhexidine gluconate
Oral rinse of either 0.12% Chlorhexidine Gluconate oral rinse to test the safety/efficacy of 0.12% Chlorhexidine Gluconate oral rinse in decolonizing the oropharynx of children colonized with S. aureus.
DRUGSaline Placebo
Placebo saline oral rinse to to test the safety/efficacy of 0.12% Chlorhexidine Gluconate oral rinse in decolonizing the oropharynx of children colonized with S. aureus.
Sponsors
Thrasher Research Fund
Lundquist Institute for Biomedical Innovation at Harbor-UCLA Medical Center
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)
Eligibility
Sex/Gender
ALL
Age
5 Years to 18 Years
Healthy volunteers
No
Inclusion criteria
1. History of skin or soft tissue infection that occurred between 1 month and 5 years ago, regardless of whether antibiotics were given, as per patient report 2. Age \> 5 years and \< 18 years. 3. Able to gargle as assessed by verbal question. 4. Willing and able to undergo nares and oropharyngeal swabbing. 5. Able to come to the research clinic for study follow-up visits for the study period.
Exclusion criteria
1. Current suspected or confirmed infection requiring systemic antibiotics. 2. Receipt of systemic antibiotics in the prior 28 days. 3. Plans for administration or likely receipt of systemic antibiotics in the next 28 days (e.g., if the patient suffers from recurrent infections such as otitis media or has a planned surgery that requires prophylactic antibiotics). 4. Plans for hospitalization or likely hospitalization in the next 28 days (e.g., if the patient suffers from recurrent infections) 5. Any of the following in the prior 6 months: hemodialysis, peritoneal dialysis, central venous catheter placement, and systemic chemotherapy for cancer, any immune-compromising condition. 6. Previous participation in the study. 7. Pregnancy (all female subjects of childbearing age will be given a pregnancy test prior to enrollment).
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Number of Participants With Eradiction of S. Aureus From the Oropharyngeal at 7 Days | 7 days | The primary endpoint is eradication of S. aureus oropharyngeal colonization at 7 days using an intention to treat (ITT) model. . |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Number of Participants Eradication of S. Aureus Oropharyngeal Colonization at 28 Days | 28 days | Secondary outcome is eradication of S. aureus oropharyngeal colonization at 28 days using an intention to treat (ITT) model. |
| Number of Participants With Persistent Same Strain of S. Aureus Genetic Backgrounds at 28 Days | 28 days | We characterized isolates associated with breakthrough of oropharyngeal colonization. Here we show the breakthrough isolates of the same strain at 28 days. |
| Number of Participants With Persistent Different Strain of S. Aureus Genetic Backgrounds at 28 Days | 28 days | We characterized isolates associated with breakthrough of oropharyngeal colonization. Here we show the breakthrough isolates of different strains at 28 days. |
Countries
United States
Participant flow
Participants by arm
| Arm | Count |
|---|---|
| 0.12% Chlorhexidine Gluconate Oral Rinse Randomized to 15mL 0.12% Chlorhexidine Gluconate oral rinse, to be used twice daily for 60 seconds for 7 days.
Chlorhexidine gluconate: Oral rinse of either 0.12% Chlorhexidine Gluconate oral rinse to test the safety/efficacy of 0.12% Chlorhexidine Gluconate oral rinse in decolonizing the oropharynx of children colonized with S. aureus. | 33 |
| Saline Placebo Oral Rinse Randomized to 15mL saline placebo oral rinse, to be used twice daily for 60 seconds for 7 days.
Saline Placebo: Placebo saline oral rinse to to test the safety/efficacy of 0.12% Chlorhexidine Gluconate oral rinse in decolonizing the oropharynx of children colonized with S. aureus. | 34 |
| Total | 67 |
Baseline characteristics
| Characteristic | Total | 0.12% Chlorhexidine Gluconate Oral Rinse | Saline Placebo Oral Rinse |
|---|---|---|---|
| Age, Categorical <=18 years | 67 Participants | 33 Participants | 34 Participants |
| Age, Categorical >=65 years | 0 Participants | 0 Participants | 0 Participants |
| Age, Categorical Between 18 and 65 years | 0 Participants | 0 Participants | 0 Participants |
| Age, Continuous | 11 years STANDARD_DEVIATION 11.7 | 11 years STANDARD_DEVIATION 11.7 | 12.4 years STANDARD_DEVIATION 11.7 |
| Race/Ethnicity, Customized Asian/Pacific Islander | 3 Participants | 1 Participants | 2 Participants |
| Race/Ethnicity, Customized Black/African American | 4 Participants | 3 Participants | 1 Participants |
| Race/Ethnicity, Customized other | 1 Participants | 0 Participants | 1 Participants |
| Race/Ethnicity, Customized White Hispanic | 58 Participants | 29 Participants | 29 Participants |
| Race/Ethnicity, Customized White Not Hispanic | 1 Participants | 0 Participants | 1 Participants |
| Region of Enrollment United States | 67 participants | 33 participants | 34 participants |
| Sex: Female, Male Female | 27 Participants | 14 Participants | 13 Participants |
| Sex: Female, Male Male | 40 Participants | 19 Participants | 21 Participants |
Adverse events
| Event type | EG000 affected / at risk | EG001 affected / at risk |
|---|---|---|
| deaths Total, all-cause mortality | 0 / 33 | 0 / 34 |
| other Total, other adverse events | 1 / 33 | 1 / 34 |
| serious Total, serious adverse events | 0 / 33 | 0 / 34 |
Outcome results
Primary
Number of Participants With Eradiction of S. Aureus From the Oropharyngeal at 7 Days
The primary endpoint is eradication of S. aureus oropharyngeal colonization at 7 days using an intention to treat (ITT) model. .
Time frame: 7 days
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| 0.12% Chlorhexidine Gluconate Oral Rinse | Number of Participants With Eradiction of S. Aureus From the Oropharyngeal at 7 Days | 18 Participants |
| Saline Placebo Oral Rinse | Number of Participants With Eradiction of S. Aureus From the Oropharyngeal at 7 Days | 7 Participants |
Secondary
Number of Participants Eradication of S. Aureus Oropharyngeal Colonization at 28 Days
Secondary outcome is eradication of S. aureus oropharyngeal colonization at 28 days using an intention to treat (ITT) model.
Time frame: 28 days
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| 0.12% Chlorhexidine Gluconate Oral Rinse | Number of Participants Eradication of S. Aureus Oropharyngeal Colonization at 28 Days | 13 Participants |
| Saline Placebo Oral Rinse | Number of Participants Eradication of S. Aureus Oropharyngeal Colonization at 28 Days | 5 Participants |
Secondary
Number of Participants With Persistent Different Strain of S. Aureus Genetic Backgrounds at 28 Days
We characterized isolates associated with breakthrough of oropharyngeal colonization. Here we show the breakthrough isolates of different strains at 28 days.
Time frame: 28 days
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| 0.12% Chlorhexidine Gluconate Oral Rinse | Number of Participants With Persistent Different Strain of S. Aureus Genetic Backgrounds at 28 Days | 4 Participants |
| Saline Placebo Oral Rinse | Number of Participants With Persistent Different Strain of S. Aureus Genetic Backgrounds at 28 Days | 7 Participants |
Secondary
Number of Participants With Persistent Same Strain of S. Aureus Genetic Backgrounds at 28 Days
We characterized isolates associated with breakthrough of oropharyngeal colonization. Here we show the breakthrough isolates of the same strain at 28 days.
Time frame: 28 days
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| 0.12% Chlorhexidine Gluconate Oral Rinse | Number of Participants With Persistent Same Strain of S. Aureus Genetic Backgrounds at 28 Days | 4 Participants |
| Saline Placebo Oral Rinse | Number of Participants With Persistent Same Strain of S. Aureus Genetic Backgrounds at 28 Days | 11 Participants |