StaphylococcusPhase 2NCT02967432
Mupirocin to Reduce Staphylococcus Aureus Colonization in Infants Hospitalized in a NICU
A Phase 2 study testing Mupirocin Topical Ointment and Petroleum Jelly in people with Staphylococcus, run by Crouse Hospital at 1 site in United States.
Trial summary
The purpose of this study is to determine whether or not mupirocin treatment results in S. aureus decolonization in affected NICU patients. Read more about this study
- Who is it for?
- Any age
- Conditions the study is for
- Staphylococcus
- What is being tested?
- Mupirocin Topical Ointment and Petroleum Jelly
- Could I receive a placebo?
- Yes, some participants may receive a placebo
- How many people
- 216 participants
- Where
- 1 siteUnited States
- Study dates
- Oct 2016to Dec 2019
- Phase
- Phase 2
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages Any age
- All sexes
- No healthy volunteers
- Child, Adult, Older adult
Who may be able to join
- Infants admitted to Crouse Hospital NICU with MSSA/MRSA colonization that have parental consent for participation obtained within 2 days of their initial positive screen.
Who cannot join
- Any infant with an active or previous S. aureus infection at time of initial positive S. aureus colonization screen.
- Any infant with a condition thought to be fatal/irreversible (pulmonary hypoplasia, chromosomal/genetic syndromes, fatal cardiac anomalies).
- Any infant with a congenital condition that would prevent specimen collection or treatment application (cleft lip/palate, choanal atresia, abdominal wall defects, imperforate anus, etc.).
- Sufficient length of NICU admission will be necessary to adequately measure the primary outcome. Therefore, enrolled patients will only be included in data analysis if they remain in the NICU until after at least one subsequent MSSA/MRSA screening is performed following completion of their initial treatment course with either mupirocin or placebo.
Trial locations and contacts
1 site in 1 country.
United States1 site
Crouse Hospital - Neonatal Intensive Care Unit
Syracuse, New York, 13210
About this study
Official title: Randomized Controlled Trial of Mupirocin to Reduce Staphylococcus Aureus Colonization in Infants Hospitalized in a Neonatal Intensive Care Unit
The purpose of this study is to determine whether or not mupirocin treatment results in S. aureus decolonization in affected NICU patients.
Read the detailed description
This randomized controlled trial of mupirocin treatment of MSSA- and MRSA-colonized infants aims to determine whether or not mupirocin treatment results in S. aureus decolonization in affected NICU patients. MSSA- or MRSA-colonized patients who enroll in the study will be randomized to either a treatment group (treatment with mupirocin) or control group (treatment with placebo). A combination of active surveillance and targeted decolonization will qualitatively and quantitatively enable assessment of any changes in S. aureus colonization in study patients. The primary outcome measure will be the number of MSSA/MRSA patient colonization days in the treatment versus control groups. Secondary outcome measures will include the proportion of persistently colonized patients at each subsequent weekly screening interval in the treatment versus control group, incidence and timing of MSSA/MRSA recolonization in the treatment group, incidence of invasive infections with S. aureus in the treatment versus control group, incidence of mupirocin-resistance in treatment versus control group, and incidence of MSSA/MRSA colonization after NICU discharge in the treatment versus control group.
STUDY PROCEDURES
Current standard of care in the NICU includes active universal screening of all admitted patients weekly for MSSA/MRSA colonization and contact precautions for MRSA-positive patients. No universal or targeted decolonization procedures are currently utilized. NICU patients who screen positive for MSSA/MRSA colonization will be approached for participation in this study and consent will be obtained from a parent within 2 days of the initial positive screening result by a neonatologist. At time of enrollment, patients will be randomized to either the treatment or control group. The pharmacy team will assign randomization; all NICU staff will be blinded to the patient's study group assignments throughout their admission. The treatment group will receive mupirocin ointment applied twice daily inside the nares and to the skin around the umbilicus for five days. The control group will receive a placebo ointment (petroleum jelly) applied in an identical fashion. The control group will not receive mupirocin ointment at any time, regardless of colonization status. If patients have recurrent positive MSSA/MRSA screens during the study, they may receive additional identical courses of treatment with either mupirocin or placebo based on their study group assignment.
The mupirocin and placebo petroleum jelly ointments will be supplied by the Crouse Hospital pharmacy and sent to the NICU daily for twice daily application by the nursing staff. Both groups will receive a ½ inch ribbon topical application of mupirocin or petroleum jelly ointment according to their assignment around the umbilicus and a ½ inch ribbon inside each nare. The neonatal nursing staff will receive appropriate education regarding the application technique and study protocol prior to study initiation. The cost of the mupirocin and placebo ointments will be paid for by Neonatal Associates of Central New York, LLC, and patients will not receive any fee for this service.
Colonization with MSSA/MRSA will be screened weekly on Mondays, in line with current Crouse Hospital NICU standard of care. MSSA/MRSA screening is performed by polymerase chain reaction (PCR). Sample collection involves swabbing an infant's nares, umbilicus, and groin with a cotton-tipped applicator. The swab tip is then sent to the Crouse Hospital Laboratory for Staphylococcus species identification. There will be no additional costs associated with these screenings, as this is already standard of care. Mupirocin resistance will be assessed by disk diffusion assay with E-test methodology to determine MICs. The costs associated with this additional test will be paid for by Neonatal Associates of Central New York, LLC, and patients will not receive any fee for this service. An additional MSSA/MRSA screen will be performed approximately 2 months after discharge at a patient's primary care physicians' office visit. Sample collection procedures will be identical to the screens performed at Crouse, and the screens will be sent to Laboratory Alliance of Central New York's Microbiology Department for testing. Results will be made available to the principal investigator. The costs associated with this additional outpatient screening test will be paid for by Neonatal Associates of Central New York, LLC, and patients will not receive any fee for this service.
Routine Crouse Hospital NICU policies regarding the use of contact precautions for any MRSA colonized infant will continue during the study period. If an infant enrolled in the study displays signs or symptoms concerning for infection, diagnostic evaluation and treatment will be guided by the attending neonatologist, not deviating from the current NICU standard of care. Parents are notified if their infant screens positive for MRSA colonization and if any diagnostic evaluation was performed on their infant. Current standards of infection prevention, such as aggressive and consistent hand hygiene, sterile procedure policies, etc. will be continued during this study.
Baseline patient demographics and clinical characteristics and outcomes will be collected on every study subject, including: birth weight, sex, gestational age, birth hospital, mode of delivery, maternal age, length of rupture of membranes, chorioamnionitis, documented maternal MRSA history when available, maternal antibiotic exposure, maternal drug abuse history, respiratory support throughout hospitalization, central line access, number of days on TPN, maternal breast milk and/or formula use, gavage feeding, surgery, grade III/IV intraventricular hemorrhage (IVH), necrotizing enterocolitis (NEC), spontaneous intestinal perforation (SIP), clinical condition and gestational age at time of any infectious evaluation, description of any positive infection (cerebrospinal fluid, blood, urine, pustule, abscess, osteomyelitis, endocarditis), antibiotic exposure (agent, antibiotic days), length of hospital stay, discharge disposition, and MSSA/MRSA colonization screening results.
The number of MSSA/MRSA patient colonization days will be determined and compared between the treatment and control groups. The proportion of persistently colonized, decolonized, and recolonized study subjects at each subsequent weekly screening interval in each study group will be determined and compared. The incidence and timing of MSSA/MRSA recolonization following decolonization with mupirocin will be determined. The incidence of nosocomial sepsis and invasive infections with any organisms will be determined and compared between the two groups. The incidence of mupirocin resistance in each group will be compared. The incidence of MSSA/MRSA colonization after discharge based on the outpatient screenings will be compared.
An independent study monitoring committee, composed of a pharmacist and an attending neonatologist (not the principal investigator), will meet after the first 30 patients are enrolled and periodically after the first review to ensure the safety of this study protocol for the duration of this study.
Rates of S. aureus colonization and infection during the study period will also be compared with historical rates from the Crouse Hospital NICU to ensure that there was not some other largely unanticipated change during the study period.
All study data will be compiled into an electronic database, which will be kept in a secure password-protected computer in the principal investigator's locked office on the ninth floor of Crouse Hospital. The study subjects' personal health information including name, date of birth, and medical record numbers will be used to identify subjects, and their study information will be part of their medical record. A copy of the data collection form and data analysis form will be submitted along with this protocol and application.
STATISTICAL METHODS, DATA ANALYSIS AND INTERPRETATION
Statistical analyses will include a descriptive phase to assess the frequencies of all variables and an analytic phase to evaluate the associations between methicillin-sensitivity or resistance status and the patient's gestational age, gender, birth weight, discharge diagnoses, discharge disposition, length of NICU stay, or presence/type of underlying condition, treatments, or clinical outcomes. Pearson's X2 test will be used to compare categorical variable counts/frequencies between the treatment and control groups. The two-sample t-test will be used for continuous variables with normal distribution to test differences between means. Appropriate alternatives, such as Wilcoxon rank sum, will be used if data violate t-test assumptions. The two-proportion z-test will be used to assess differences between two proportions. All hypothesis testing will be 2-tailed with a P ≤ 0.05 considered statistically significant. An analyst for statistical support has been involved with the study design, power analysis, and sample size calculation. She will remain involved throughout the study period and will assist with data analysis.
Neonatal MSSA/MRSA patient colonization days data from the Crouse Hospital NICU was used for sample size calculations. Approximately 12-15 new cases of MSSA- or MRSA-colonization occur each month, with a mean of 21.5 patient colonization days (standard deviation 20 days). A two-sample t-test with 95% confidence interval, power of 80, and hypothesized reduction of 40% (8 patient colonization days), suggests a sample size of 98 patients per group, or a total of approximately 200 patients in the study.
All study personnel, aside from the pharmacy staff who will randomize patients, will be blinded regarding patients' study group allocation until after discharge from the Crouse Hospital NICU. At time of discharge, the pharmacy will notify the principal investigator of each patient's study group allocation so that data analysis by treatment group can occur.
- Conditions
- Staphylococcus
- Being tested
- Mupirocin Topical Ointment, Petroleum Jelly
- Keywords
- Staphylococcus aureus, Staphylococcal colonization, Staphylococcal infection, Mupirocin, Mupirocin-resistance
- Medical subject headings
- Staphylococcal Infections
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Mupirocin Topical OintmentDrug
Mupirocin ointment 1/2 inch ribbon applied topically to each nare and umbilicus twice daily for 5 days; repeat treatment courses possible.
Petroleum JellyDrug
Petroleum jelly ointment 1/2 inch ribbon applied topically to each nare and umbilicus twice daily for 5 days; repeat treatment courses possible.
| Study group | Role | What they receive |
|---|---|---|
| Mupirocin | Experimental | Not described Receives: Drug: Mupirocin Topical Ointment |
| Petroleum jelly | Placebo comparator | Not described Receives: Drug: Petroleum Jelly |
What is being measured
The primary outcome is the main question the study is designed to answer.
Decolonization efficacy
Compare the number of S. aureus patient colonization days between treatment versus control group
Measured: Remaining length of NICU admission status post positive screening culture, approximately between 7 to 365 days
Secondary outcomes (5)
Trajectory of decolonization efficacy
Compare the proportions of persistently colonized, decolonized, and recolonized study subjects at each subsequent weekly screening interval in treatment versus control group
Measured: Remaining length of NICU admission status post positive screening culture, approximately between 7 to 365 days
Incidence of recolonization
Determine the incidence and timing of recolonization with S. aureus following decolonization within the treatment group
Measured: Remaining length of NICU admission status post positive screening culture, approximately between 7 to 365 days
Incidence of S. aureus infection
Determine and compare the incidence of nosocomial invasive S. aureus infection in treatment versus control group
Measured: Remaining length of NICU admission status post positive screening culture, approximately between 7 to 365 days
Incidence of mupirocin-resistance
Determine the incidence of mupirocin-resistance in S. aureus isolates from treatment versus control group
Measured: Remaining length of NICU admission status post positive screening culture, approximately between 7 to 365 days
Long-term decolonization efficacy
Determine and compare the incidence of S. aureus colonization between 1-2 months after discharge between treatment versus control group
Measured: Within 2 months of discharge from NICU
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted18 Nov 2016 (estimated)
- Study startOct 2016
- Primary completionDec 2019
- Study completionDec 2019
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (1)Papers the sponsor has linked to this study.
- Other trials for StaphylococcusStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase 2
- Primary purpose
- Prevention
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Quadruple blind
- Who is masked
- Participant, Care provider, Investigator, Outcomes assessor
- Enrolment
- 216 participants (actual)
Sponsor and investigators
- Lead sponsor
- Crouse Hospital
- Sponsor type
- University, hospital or other
- Collaborators
- Jana Shaw, MD, Steven Gross, MD, David Martin, RN, Dale Franz, RPh, Rachel Carey
- Responsible party
- Principal investigator, Melissa Nelson, Crouse Hospital
- Investigators
- Melissa U Nelson, MD, Principal investigator, Crouse Hospital
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT02967432
- Sponsor's protocol ID
- Crouse Hospital 2016.0125
- Status last verified
- Dec 2020
- First submitted
- 15 Nov 2016
- Last updated
- 21 Dec 2020
- Results posted
- No
- Data monitoring committee
- Yes
- Individual data sharing
- No
Publications
Nelson MU, Shaw J, Gross SJ. Randomized Placebo-Controlled Trial of Topical Mupirocin to Reduce Staphylococcus aureus Colonization in Infants in the Neonatal Intensive Care Unit. J Pediatr. 2021 Sep;236:70-77. doi: 10.1016/j.jpeds.2021.05.042. Epub 2021 May 21.
PubMed 34023342
Study at a glance
From the registry record, last updated by the sponsor on 21 Dec 2020. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Randomized Controlled Trial of Mupirocin to Reduce Staphylococcus Aureus Colonization in Infants Hospitalized in a Neonatal Intensive Care Unit
- ClinicalTrials.gov ID
- NCT02967432
- Acronym / sponsor ID
- Crouse Hospital 2016.0125
- Conditions
- Staphylococcus
- Keywords
- Staphylococcus aureus, Staphylococcal colonization, Staphylococcal infection, Mupirocin, Mupirocin-resistance
- Phase
- Phase 2
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 216 participants (actual)
- Lead sponsor
- Crouse HospitalUniversity, hospital or other
- Collaborators
- Jana Shaw, MD, Steven Gross, MD, David Martin, RN, Dale Franz, RPh, Rachel Carey
- Study start
- Oct 2016 (actual)
- Primary completion
- Dec 2019 (actual)
- Study completion
- Dec 2019 (actual)
- First posted
- 18 Nov 2016 (estimated)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The purpose of this study is to determine whether or not mupirocin treatment results in S. aureus decolonization in affected NICU patients.
Detailed description
This randomized controlled trial of mupirocin treatment of MSSA- and MRSA-colonized infants aims to determine whether or not mupirocin treatment results in S. aureus decolonization in affected NICU patients. MSSA- or MRSA-colonized patients who enroll in the study will be randomized to either a treatment group (treatment with mupirocin) or control group (treatment with placebo). A combination of active surveillance and targeted decolonization will qualitatively and quantitatively enable assessment of any changes in S. aureus colonization in study patients. The primary outcome measure will be the number of MSSA/MRSA patient colonization days in the treatment versus control groups. Secondary outcome measures will include the proportion of persistently colonized patients at each subsequent weekly screening interval in the treatment versus control group, incidence and timing of MSSA/MRSA recolonization in the treatment group, incidence of invasive infections with S. aureus in the treatment versus control group, incidence of mupirocin-resistance in treatment versus control group, and incidence of MSSA/MRSA colonization after NICU discharge in the treatment versus control group.
STUDY PROCEDURES
Current standard of care in the NICU includes active universal screening of all admitted patients weekly for MSSA/MRSA colonization and contact precautions for MRSA-positive patients. No universal or targeted decolonization procedures are currently utilized. NICU patients who screen positive for MSSA/MRSA colonization will be approached for participation in this study and consent will be obtained from a parent within 2 days of the initial positive screening result by a neonatologist. At time of enrollment, patients will be randomized to either the treatment or control group. The pharmacy team will assign randomization; all NICU staff will be blinded to the patient's study group assignments throughout their admission. The treatment group will receive mupirocin ointment applied twice daily inside the nares and to the skin around the umbilicus for five days. The control group will receive a placebo ointment (petroleum jelly) applied in an identical fashion. The control group will not receive mupirocin ointment at any time, regardless of colonization status. If patients have recurrent positive MSSA/MRSA screens during the study, they may receive additional identical courses of treatment with either mupirocin or placebo based on their study group assignment.
The mupirocin and placebo petroleum jelly ointments will be supplied by the Crouse Hospital pharmacy and sent to the NICU daily for twice daily application by the nursing staff. Both groups will receive a ½ inch ribbon topical application of mupirocin or petroleum jelly ointment according to their assignment around the umbilicus and a ½ inch ribbon inside each nare. The neonatal nursing staff will receive appropriate education regarding the application technique and study protocol prior to study initiation. The cost of the mupirocin and placebo ointments will be paid for by Neonatal Associates of Central New York, LLC, and patients will not receive any fee for this service.
Colonization with MSSA/MRSA will be screened weekly on Mondays, in line with current Crouse Hospital NICU standard of care. MSSA/MRSA screening is performed by polymerase chain reaction (PCR). Sample collection involves swabbing an infant's nares, umbilicus, and groin with a cotton-tipped applicator. The swab tip is then sent to the Crouse Hospital Laboratory for Staphylococcus species identification. There will be no additional costs associated with these screenings, as this is already standard of care. Mupirocin resistance will be assessed by disk diffusion assay with E-test methodology to determine MICs. The costs associated with this additional test will be paid for by Neonatal Associates of Central New York, LLC, and patients will not receive any fee for this service. An additional MSSA/MRSA screen will be performed approximately 2 months after discharge at a patient's primary care physicians' office visit. Sample collection procedures will be identical to the screens performed at Crouse, and the screens will be sent to Laboratory Alliance of Central New York's Microbiology Department for testing. Results will be made available to the principal investigator. The costs associated with this additional outpatient screening test will be paid for by Neonatal Associates of Central New York, LLC, and patients will not receive any fee for this service.
Routine Crouse Hospital NICU policies regarding the use of contact precautions for any MRSA colonized infant will continue during the study period. If an infant enrolled in the study displays signs or symptoms concerning for infection, diagnostic evaluation and treatment will be guided by the attending neonatologist, not deviating from the current NICU standard of care. Parents are notified if their infant screens positive for MRSA colonization and if any diagnostic evaluation was performed on their infant. Current standards of infection prevention, such as aggressive and consistent hand hygiene, sterile procedure policies, etc. will be continued during this study.
Baseline patient demographics and clinical characteristics and outcomes will be collected on every study subject, including: birth weight, sex, gestational age, birth hospital, mode of delivery, maternal age, length of rupture of membranes, chorioamnionitis, documented maternal MRSA history when available, maternal antibiotic exposure, maternal drug abuse history, respiratory support throughout hospitalization, central line access, number of days on TPN, maternal breast milk and/or formula use, gavage feeding, surgery, grade III/IV intraventricular hemorrhage (IVH), necrotizing enterocolitis (NEC), spontaneous intestinal perforation (SIP), clinical condition and gestational age at time of any infectious evaluation, description of any positive infection (cerebrospinal fluid, blood, urine, pustule, abscess, osteomyelitis, endocarditis), antibiotic exposure (agent, antibiotic days), length of hospital stay, discharge disposition, and MSSA/MRSA colonization screening results.
The number of MSSA/MRSA patient colonization days will be determined and compared between the treatment and control groups. The proportion of persistently colonized, decolonized, and recolonized study subjects at each subsequent weekly screening interval in each study group will be determined and compared. The incidence and timing of MSSA/MRSA recolonization following decolonization with mupirocin will be determined. The incidence of nosocomial sepsis and invasive infections with any organisms will be determined and compared between the two groups. The incidence of mupirocin resistance in each group will be compared. The incidence of MSSA/MRSA colonization after discharge based on the outpatient screenings will be compared.
An independent study monitoring committee, composed of a pharmacist and an attending neonatologist (not the principal investigator), will meet after the first 30 patients are enrolled and periodically after the first review to ensure the safety of this study protocol for the duration of this study.
Rates of S. aureus colonization and infection during the study period will also be compared with historical rates from the Crouse Hospital NICU to ensure that there was not some other largely unanticipated change during the study period.
All study data will be compiled into an electronic database, which will be kept in a secure password-protected computer in the principal investigator's locked office on the ninth floor of Crouse Hospital. The study subjects' personal health information including name, date of birth, and medical record numbers will be used to identify subjects, and their study information will be part of their medical record. A copy of the data collection form and data analysis form will be submitted along with this protocol and application.
STATISTICAL METHODS, DATA ANALYSIS AND INTERPRETATION
Statistical analyses will include a descriptive phase to assess the frequencies of all variables and an analytic phase to evaluate the associations between methicillin-sensitivity or resistance status and the patient's gestational age, gender, birth weight, discharge diagnoses, discharge disposition, length of NICU stay, or presence/type of underlying condition, treatments, or clinical outcomes. Pearson's X2 test will be used to compare categorical variable counts/frequencies between the treatment and control groups. The two-sample t-test will be used for continuous variables with normal distribution to test differences between means. Appropriate alternatives, such as Wilcoxon rank sum, will be used if data violate t-test assumptions. The two-proportion z-test will be used to assess differences between two proportions. All hypothesis testing will be 2-tailed with a P ≤ 0.05 considered statistically significant. An analyst for statistical support has been involved with the study design, power analysis, and sample size calculation. She will remain involved throughout the study period and will assist with data analysis.
Neonatal MSSA/MRSA patient colonization days data from the Crouse Hospital NICU was used for sample size calculations. Approximately 12-15 new cases of MSSA- or MRSA-colonization occur each month, with a mean of 21.5 patient colonization days (standard deviation 20 days). A two-sample t-test with 95% confidence interval, power of 80, and hypothesized reduction of 40% (8 patient colonization days), suggests a sample size of 98 patients per group, or a total of approximately 200 patients in the study.
All study personnel, aside from the pharmacy staff who will randomize patients, will be blinded regarding patients' study group allocation until after discharge from the Crouse Hospital NICU. At time of discharge, the pharmacy will notify the principal investigator of each patient's study group allocation so that data analysis by treatment group can occur.
Study design
- Primary purpose
- Prevention
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Quadruple blind (participant, care provider, investigator, outcomes assessor)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Mupirocin | Experimental | Drug: Mupirocin Topical Ointment |
| Petroleum jelly | Placebo comparator | Drug: Petroleum Jelly |
Who may qualify
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Child, Adult, Older adult
Key inclusion criteria (1 listed)
- Infants admitted to Crouse Hospital NICU with MSSA/MRSA colonization that have parental consent for participation obtained within 2 days of their initial positive screen.
Key exclusion criteria (4 listed)
- Any infant with an active or previous S. aureus infection at time of initial positive S. aureus colonization screen.
- Any infant with a condition thought to be fatal/irreversible (pulmonary hypoplasia, chromosomal/genetic syndromes, fatal cardiac anomalies).
- Any infant with a congenital condition that would prevent specimen collection or treatment application (cleft lip/palate, choanal atresia, abdominal wall defects, imperforate anus, etc.).
- Sufficient length of NICU admission will be necessary to adequately measure the primary outcome. Therefore, enrolled patients will only be included in data analysis if they remain in the NICU until after at least one subsequent MSSA/MRSA screening is performed following completion of their initial treatment course with either mupirocin or placebo.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Mupirocin Topical OintmentMupirocin ointment 1/2 inch ribbon applied topically to each nare and umbilicus twice daily for 5 days; repeat treatment courses possible. | Drug | Mupirocin |
| Petroleum JellyPetroleum jelly ointment 1/2 inch ribbon applied topically to each nare and umbilicus twice daily for 5 days; repeat treatment courses possible. | Drug | Petroleum jelly |
Primary outcome
Decolonization efficacy
Time frame: Remaining length of NICU admission status post positive screening culture, approximately between 7 to 365 days
Compare the number of S. aureus patient colonization days between treatment versus control group
5 secondary outcomes
Trajectory of decolonization efficacy
Time frame: Remaining length of NICU admission status post positive screening culture, approximately between 7 to 365 days
Incidence of recolonization
Time frame: Remaining length of NICU admission status post positive screening culture, approximately between 7 to 365 days
Incidence of S. aureus infection
Time frame: Remaining length of NICU admission status post positive screening culture, approximately between 7 to 365 days
Incidence of mupirocin-resistance
Time frame: Remaining length of NICU admission status post positive screening culture, approximately between 7 to 365 days
Long-term decolonization efficacy
Time frame: Within 2 months of discharge from NICU
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 21 Dec 2020.
- Derived from this study: PubMed 34023342Nelson MU, Shaw J, Gross SJ. Randomized Placebo-Controlled Trial of Topical Mupirocin to Reduce Staphylococcus aureus Colonization in Infants in the Neonatal Intensive Care Unit. J Pediatr. 2021 Sep;236:70-77. doi: 10.1016/j.jpeds.2021.05.042. Epub 2021 May 21.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Melissa U Nelson, MD principal investigator
Crouse Hospital
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 2 study testing Mupirocin Topical Ointment and Petroleum Jelly in people with Staphylococcus, run by Crouse Hospital at 1 site in United States.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 1 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 21 Dec 2020. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
What does this phase mean?
Phase 2 studies give the treatment to a larger group to see whether it has the intended effect and to keep checking safety.
Not every study follows the same path, and some studies (observational studies, device studies) have no phase.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Decolonization efficacy (time frame: Remaining length of NICU admission status post positive screening culture, approximately between 7 to 365 days). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT02967432, which also lists 1 linked publication.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 21 Dec 2020.