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| ID | Type | Description | Link |
|---|---|---|---|
| R01HS022872 | U.S. AHRQ Grant/Contract | View source |
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| Name | Class |
|---|---|
| Agency for Healthcare Research and Quality (AHRQ) | FED |
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This trial will test the hypothesis that treating parents of neonates requiring NICU care with intranasal mupirocin and topical chlorhexidine bathing will reduce the spread of S. aureus from parents to neonates.
The TREAT PARENTS Trial, or Treating Parents to Reduce NICU Transmission of S. aureus, is a placebo-controlled, double-masked, randomized clinical trial to test the hypothesis that treatment of S. aureus colonized parents with intranasal mupirocin and topical chlorhexidine gluconate antisepsis will decrease neonatal S. aureus acquisition. All neonates admitted to the Johns Hopkins Hospital and Johns Hopkins Bayview Medical Center NICUs will be pre-screened and parents will be approached for enrollment in the study. After consent and baseline screening, 400 neonate-parent pairs will be randomized; only neonates who have a parent colonized with S. aureus will be randomized. Parents will receive a 5 day treatment with intranasal mupirocin plus topical chlorhexidine gluconate antisepsis or placebo.
After recruitment and informed consent, parents will undergo pre-randomization screening. If both parents screen negative for S. aureus colonization, the neonate will be ineligible for the randomization and parents will be informed that the parents are not colonized at that time with S. aureus. If either parent screens positive for S. aureus, then both parents as a pair will be eligible for randomization to one of the two possible masked treatment arms. The neonate-parent "pair" will be the unit of randomization and each parent will be allocated to the same group if both consent.
After the baseline neonate testing for S. aureus colonization, repeat testing will be performed every 7 days for the neonates until the neonate acquires S. aureus colonization or is discharged from the NICU.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Mupirocin and Chlorhexidine | Active Comparator | Participants will apply 2% intranasal mupirocin twice a day for five days and cleanse with 2% chlorhexidine cloths once a day for five days. |
|
| Placebo ointment and placebo cloths | Placebo Comparator | Participants will apply 2% petrolatum intranasal placebo ointment twice a day for five days and cleanse with 2% non-medicated soap placebo cloths once a day for five days. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Mupirocin and Chlorhexidine | Drug |
|
| |
| Measure | Description | Time Frame |
|---|---|---|
| Number of Neonatal Infections With a S. Aureus Strain That is Concordant to Parental S. Aureus Strain | Primary outcome is neonatal acquisition of S. aureus strain that is concordant to parental S. aureus strain as determined by periodic surveillance cultures or a culture collected during routine clinical care that grows S. aureus. Survival analysis techniques will be used to compare the hazard of concordant colonization comparing Treatment and Control Groups. | Up to 90 days |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Aaron Milstone, MD, MHS | Johns Hopkins University | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Johns Hopkins Bayview Medical Center | Baltimore | Maryland | 21224 | United States | ||
| Johns Hopkins Hospital |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 31886828 | Derived | Milstone AM, Voskertchian A, Koontz DW, Khamash DF, Ross T, Aucott SW, Gilmore MM, Cosgrove SE, Carroll KC, Colantuoni E. Effect of Treating Parents Colonized With Staphylococcus aureus on Transmission to Neonates in the Intensive Care Unit: A Randomized Clinical Trial. JAMA. 2020 Jan 28;323(4):319-328. doi: 10.1001/jama.2019.20785. | |
| 26353875 | Derived | Milstone AM, Koontz DW, Voskertchian A, Popoola VO, Harrelson K, Ross T, Aucott SW, Gilmore MM, Carroll KC, Colantuoni E. Treating Parents to Reduce NICU Transmission of Staphylococcus aureus (TREAT PARENTS) trial: protocol of a multisite randomised, double-blind, placebo-controlled trial. BMJ Open. 2015 Sep 9;5(9):e009274. doi: 10.1136/bmjopen-2015-009274. |
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| ID | Title | Description |
|---|---|---|
| FG000 | Mupirocin and Chlorhexidine | Participants will apply 2% intranasal mupirocin twice a day for five days and cleanse with 2% chlorhexidine cloths once a day for five days. Mupirocin and Chlorhexidine |
| FG001 | Placebo Ointment and Placebo Cloths | Participants will apply 2% petrolatum intranasal placebo ointment twice a day for five days and cleanse with 2% non-medicated soap placebo cloths once a day for five days. Placebo ointment and placebo cloths |
| Title | Milestones | Reasons Not Completed | ||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Overall Study |
|
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| ID | Title | Description |
|---|---|---|
| BG000 | Mupirocin and Chlorhexidine | Participants will apply 2% intranasal mupirocin twice a day for five days and cleanse with 2% chlorhexidine cloths once a day for five days. Mupirocin and Chlorhexidine |
| BG001 | Placebo Ointment and Placebo Cloths |
| Units | Counts |
|---|---|
| Participants |
|
| Title | Description | Population Description | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Denominator Units Selected | Denominators | Classes |
|---|---|---|---|---|---|---|---|---|---|
| Age, Continuous | Age of neonate at time of enrollment (days) |
| Type | Title | Description | Population Description | Reporting Status | Anticipated Posting Date | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Time Frame | Units Analyzed | Denominator Units Selected | Arm/Group Information | Denominators | Classes | Analyses | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Primary | Number of Neonatal Infections With a S. Aureus Strain That is Concordant to Parental S. Aureus Strain | Primary outcome is neonatal acquisition of S. aureus strain that is concordant to parental S. aureus strain as determined by periodic surveillance cultures or a culture collected during routine clinical care that grows S. aureus. Survival analysis techniques will be used to compare the hazard of concordant colonization comparing Treatment and Control Groups. | This outcome is being assessed in the neonate population not the mothers. 12 of the neonates in the intervention group and 6 in the placebo group were lost to follow-up and could not be included in the analysis. | Posted | Number | neonatal S. aureus infections | Up to 90 days |
|
During the 5 days of treatment
Adverse events were assessed in mothers not neonates.
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| ID | Title | Description | Deaths (Affected) | Deaths (At Risk) | Serious Events (Affected) | Serious Events (At Risk) | Other Events (Affected) | Other Events (At Risk) |
|---|---|---|---|---|---|---|---|---|
| EG000 | Mupirocin and Chlorhexidine | Participants will apply 2% intranasal mupirocin twice a day for five days and cleanse with 2% chlorhexidine cloths once a day for five days. Mupirocin and Chlorhexidine |
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| Term | Organ System | Source Vocabulary | Assessment Type | Notes | Statistical Information |
|---|---|---|---|---|---|
| Skin irritation | Skin and subcutaneous tissue disorders | Systematic Assessment |
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| Title | Organization | Phone | Extension | |
|---|---|---|---|---|
| Aaron M. Milstone, M.D., M.H.S. | Johns Hopkins Medical Institutions | 410-614-3917 | amilsto1@jhmi.edu |
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| Type | Includes Protocol | Includes SAP | Includes ICF | Document Label | Document Date | Document Uploaded Date | Document File Name |
|---|---|---|---|---|---|---|---|
| Prot_SAP | Yes | Yes | No | Study Protocol and Statistical Analysis Plan | Nov 30, 2018 | Feb 26, 2020 | Prot_SAP_000.pdf |
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| ID | Term |
|---|---|
| D013203 | Staphylococcal Infections |
| D007239 | Infections |
| ID | Term |
|---|---|
| D016908 | Gram-Positive Bacterial Infections |
| D001424 | Bacterial Infections |
| D001423 | Bacterial Infections and Mycoses |
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| ID | Term |
|---|---|
| D016712 | Mupirocin |
| D002710 | Chlorhexidine |
| C010882 | chlorhexidine gluconate |
| ID | Term |
|---|---|
| D004852 | Epoxy Compounds |
| D004988 | Ethers, Cyclic |
| D004987 | Ethers |
| D009930 | Organic Chemicals |
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| Placebo ointment and placebo cloths |
| Drug |
|
| Baltimore |
| Maryland |
| 21287 |
| United States |
Participants will apply 2% petrolatum intranasal placebo ointment twice a day for five days and cleanse with 2% non-medicated soap placebo cloths once a day for five days. Placebo ointment and placebo cloths |
| BG002 | Total | Total of all reporting groups |
This baseline measure reported is for the neonates not the parents.
| Mean |
| Standard Deviation |
| days |
|
| Sex: Female, Male | This baseline measure reported is for the neonates not the parents. | Count of Participants | Participants |
|
| Ethnicity (NIH/OMB) | This baseline measure reported is for the neonates not the parents. | Count of Participants | Participants |
|
| Race (NIH/OMB) | This baseline measure reported is for the neonates not the parents. | Count of Participants | Participants |
|
| Region of Enrollment | This baseline measure reported is for the neonates not the parents. | Count of Participants | Participants |
|
| Parent age at the time of enrollment | This is a measure for the parents. Parent demographics collected by parent interview or parent completion of form. Parents sometimes skipped questions on survey form and were not always available to capture missing demographic data that was not in the medical record. | Mean | Standard Deviation | years |
|
| Parent antibiotic use in past 6 months | Count of Participants | Participants |
|
| Parent history of mupirocin use | Count of Participants | Participants |
|
| Parent history of Staphylococcus aureus infection | Count of Participants | Participants |
|
| Level of education of parent | Count of Participants | Participants |
|
| No. of singletons | Neonates that were delivered as singletons. | This baseline measure reported is for the neonates not the parents. | Count of Participants | Participants |
|
| Birthweight of neonate | This baseline measure reported is for the neonates not the parents. | Mean | Standard Deviation | grams |
|
| Child delivery method | This baseline measure reported is for the neonates not the parents. | Count of Participants | Participants |
|
| Neonate inborn or transferred in | Inborn was defined as neonates who were born at Johns Hopkins Hospital (JHH)/Johns Hopkins Bayview Medical Center (JHBMC) instead of being transferred to JHH/JHBMC from an outside hospital or home. | This baseline measure reported is for the neonates not the parents. | Count of Participants | Participants |
|
| Gestational age at birth | This baseline measure reported is for the neonates not the parents. | Mean | Standard Deviation | weeks |
|
| Maternal antibiotic use during delivery | Neonates whose mothers reported using antibiotic during delivery. | This baseline measure reported is for the neonates not the parents. | Count of Participants | Participants |
|
| Maternal Group B Streptococcus positive | Neonates whose mothers reported testing positive for Group B Streptococcus. | This baseline measure reported is for the neonates not the parents. | Count of Participants | Participants |
|
| Maternal HIV Positive | Neonates whose mothers reported being positive for HIV. | This baseline measure reported is for the neonates not the parents. | Count of Participants | Participants |
|
| OG001 | Placebo Ointment and Placebo Cloths | Participants will apply 2% petrolatum intranasal placebo ointment twice a day for five days and cleanse with 2% non-medicated soap placebo cloths once a day for five days. Placebo ointment and placebo cloths |
|
|
| 0 |
| 147 |
| 0 |
| 147 |
| 9 |
| 147 |
| EG001 | Placebo Ointment and Placebo Cloths | Participants will apply 2% petrolatum intranasal placebo ointment twice a day for five days and cleanse with 2% non-medicated soap placebo cloths once a day for five days. Placebo ointment and placebo cloths | 0 | 160 | 0 | 160 | 16 | 160 |
| Nose irritation | Respiratory, thoracic and mediastinal disorders | Systematic Assessment |
|
| Nasal congestion | Respiratory, thoracic and mediastinal disorders | Systematic Assessment |
|
| Retained placenta | Pregnancy, puerperium and perinatal conditions | Systematic Assessment |
|
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| D011714 |
| Pyrans |
| D006573 | Heterocyclic Compounds, 1-Ring |
| D006571 | Heterocyclic Compounds |
| D005227 | Fatty Acids |
| D008055 | Lipids |
| D001645 | Biguanides |
| D006146 | Guanidines |
| D000578 | Amidines |
| Unknown or Not Reported |
|
| Native Hawaiian or Other Pacific Islander |
|
| Black or African American |
|
| White |
|
| More than one race |
|
| Unknown or Not Reported |
|
| Unreported/Unknown |
|
| Unreported/Unknown |
|
| Unreported/Unknown |
|
| Graduate degree |
|
| Unknown |
|
| Transferred from home to JHH/JHBMC |
|
| Unreported/Unknown |
|
| Unreported/Unknown |
|