Treating Parents to Reduce NICU Transmission of Staphylococcus Aureus Trial (TREAT PARENTS)
Primary Purpose
Staph Aureus Colonization, Staph Aureus Infection
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Mupirocin and Chlorhexidine
Placebo ointment and placebo cloths
Sponsored by
About this trial
This is an interventional prevention trial for Staph Aureus Colonization focused on measuring Staphylococcus aureus, Infection, Colonization, Transmission, Neonate
Eligibility Criteria
Inclusion Criteria:
- Neonate has never had a clinical or surveillance culture grow S. aureus
- Neonate was transferred from another hospital or admitted from home and had admission screening cultures for S. aureus colonization that were negative (if admission cultures were not performed, the cultures will be performed as part of the pre-randomization screening process)
- Parent(s) is(are) able to visit the child at the bedside
- Parent(s) test positive for S. aureus at screening
- Neonate has anticipated stay longer than 5 days in the NICU (if estimated stay is unclear, parents can be screened for S. aureus colonization and decision to randomize can be delayed until hospital day 3 or 4 after reassessment of anticipated stay).
- Parents is(are) willing to be randomized
- No documented or reported allergies to any agent used in either treatment regimen
- Able to perform written informed consent
Exclusion Criteria:
- Allergies to any agent used in either treatment regimen
- Neonate has had a prior clinical or surveillance culture grow S. aureus
- Neonate admitted to NICU from home and is greater than 7 days of age
- Neonate admitted to NICU from another hospital and is greater than 7 days of age
- Neonate is a ward of the State
- Not able to provide written informed consent
Sites / Locations
- Johns Hopkins Bayview Medical Center
- Johns Hopkins Hospital
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Placebo Comparator
Arm Label
Mupirocin and Chlorhexidine
Placebo ointment and placebo cloths
Arm Description
Participants will apply 2% intranasal mupirocin twice a day for five days and cleanse with 2% chlorhexidine cloths once a day for five days.
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.
Outcomes
Primary Outcome Measures
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.
Secondary Outcome Measures
Full Information
NCT ID
NCT02223520
First Posted
August 21, 2014
Last Updated
January 7, 2022
Sponsor
Johns Hopkins University
Collaborators
Agency for Healthcare Research and Quality (AHRQ)
1. Study Identification
Unique Protocol Identification Number
NCT02223520
Brief Title
Treating Parents to Reduce NICU Transmission of Staphylococcus Aureus Trial
Acronym
TREAT PARENTS
Official Title
Treating Parents to Reduce Neonatal Intensive Care Unit (NICU) Transmission of Staphylococcus Aureus
Study Type
Interventional
2. Study Status
Record Verification Date
March 2020
Overall Recruitment Status
Completed
Study Start Date
November 2014 (Actual)
Primary Completion Date
October 31, 2019 (Actual)
Study Completion Date
October 31, 2019 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Johns Hopkins University
Collaborators
Agency for Healthcare Research and Quality (AHRQ)
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
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.
Detailed Description
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.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Staph Aureus Colonization, Staph Aureus Infection
Keywords
Staphylococcus aureus, Infection, Colonization, Transmission, Neonate
7. Study Design
Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
307 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Mupirocin and Chlorhexidine
Arm Type
Active Comparator
Arm Description
Participants will apply 2% intranasal mupirocin twice a day for five days and cleanse with 2% chlorhexidine cloths once a day for five days.
Arm Title
Placebo ointment and placebo cloths
Arm Type
Placebo Comparator
Arm Description
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.
Intervention Type
Drug
Intervention Name(s)
Mupirocin and Chlorhexidine
Other Intervention Name(s)
bactroban, chlorhexidine gluconate
Intervention Type
Drug
Intervention Name(s)
Placebo ointment and placebo cloths
Primary Outcome Measure Information:
Title
Number of Neonatal Infections With a S. Aureus Strain That is Concordant to Parental S. Aureus Strain
Description
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.
Time Frame
Up to 90 days
10. Eligibility
Sex
All
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Neonate has never had a clinical or surveillance culture grow S. aureus
Neonate was transferred from another hospital or admitted from home and had admission screening cultures for S. aureus colonization that were negative (if admission cultures were not performed, the cultures will be performed as part of the pre-randomization screening process)
Parent(s) is(are) able to visit the child at the bedside
Parent(s) test positive for S. aureus at screening
Neonate has anticipated stay longer than 5 days in the NICU (if estimated stay is unclear, parents can be screened for S. aureus colonization and decision to randomize can be delayed until hospital day 3 or 4 after reassessment of anticipated stay).
Parents is(are) willing to be randomized
No documented or reported allergies to any agent used in either treatment regimen
Able to perform written informed consent
Exclusion Criteria:
Allergies to any agent used in either treatment regimen
Neonate has had a prior clinical or surveillance culture grow S. aureus
Neonate admitted to NICU from home and is greater than 7 days of age
Neonate admitted to NICU from another hospital and is greater than 7 days of age
Neonate is a ward of the State
Not able to provide written informed consent
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Aaron Milstone, MD, MHS
Organizational Affiliation
Johns Hopkins University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Johns Hopkins Bayview Medical Center
City
Baltimore
State/Province
Maryland
ZIP/Postal Code
21224
Country
United States
Facility Name
Johns Hopkins Hospital
City
Baltimore
State/Province
Maryland
ZIP/Postal Code
21287
Country
United States
12. IPD Sharing Statement
Citations:
PubMed Identifier
31886828
Citation
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.
Results Reference
derived
PubMed Identifier
26353875
Citation
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.
Results Reference
derived
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Treating Parents to Reduce NICU Transmission of Staphylococcus Aureus Trial
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