Mother to Newborn Transmission of Staphylococcus Aureus and Dynamics of S.Aureus Carriage During the First Years Life
NCT ID: NCT03064373
Last Updated: 2017-02-27
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
UNKNOWN
600 participants
OBSERVATIONAL
2008-12-17
2023-06-17
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
We aim to 1) Define the route of transmission between mother and newborn. 2) Assess the dynamics of S. aureus carriage during the first years of life and specifically determine risk factors for becoming a persistent carrier of S. aureus
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
MRSA Colonization in Peripartum Women and Their Offspring
NCT00336427
Severe Group A Streptococcus Infections in Paris, France, 2018-2023
NCT06297122
Invasive Group A Streptococcal Infection
NCT05788861
Streptococcal Infection and Respiratory Distress in Newborns
NCT00612937
A Prospective Cohort Pilot Study of the Clinical and Molecular Epidemiology of Staphylococcus Aureus in Pregnant Women at the Time of Group B Streptococcal Screening in a Large Urban Medical Center in Chicago, IL USA
NCT00532324
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
prospective cohort study which will examine the risk of exposure to S. aureus carrier mother on the outcome: S. aureus carriage by newborns following delivery and at discharge.
1. Risk of vertical transmission during delivery will be assessed by comparing a cohort of newborns to vaginal S. aureus carrier mothers to a cohort of newborns of mothers not carrying S. aureus vaginally.
2. Risk of horizontal transmission during the first days of life will be assessed by following a cohort of newborns not colonized on delivery day. The main exposure of interest is maternal nasal SA carriage.Target populations: 300 mother - newborn pairs.
Setting:
Sheba Medical Center obstetrical unit and nursery Gravid women will be recruited during antenatal visit at the Sheba medical Center, 1-4 weeks prior to labor. Women who will agree to participate and sign an informed consent will be screened for nasal and vaginal carriage of S. aureus. Newborns will be screened on delivery day and on discharge day.
Inclusion criteria:
1. Gravid women expected to deliver within 4 weeks.
2. Women who agree to participate and sign an informed consent
3. Women who are S. aureus carriers at the time of recruit.
Exclusion criteria:
1. Prolonged (\>6 days) newborn hospitalization.
2. Women who did not give birth eventually at the Sheba Medical Center.
3. Women who's newborns were not screened at least once during delivery hospitalization.
Enrollment:
300 consecutive women who are defined as S. aureus carriers (see definitions below).
Screening will include:
Stage I before discharge:
1. Women - nasal screenings:
A) On recruitment day (\~1-4 weeks before labor), B) During hospitalization for delivery. Vaginal screening will be performed during the routine gynecologic examination on delivery day.
2. Newborns - will be screened A) On birth day, at entrance to the nursery. B) On discharge day. Screening will include nasal nares, umbilical, ear and rectal swabbing on each screening while hospitalized.
3. Data collection by questionnaires filled by recruited women.
4. Data collection from medical files of the maternity ward.
Stage II after discharge until age 5 years:
1. Mothers - monthly nasal swab for 12 months.
2. Children - monthly nasal, nasopharyngeal and rectal swabs for 12 months.
3. Same screen annually until the child is 5years old.
4. Data collection by questionnaires filled by the mothers.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
FAMILY_BASED
PROSPECTIVE
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
2. Women who agree to participate and sign an informed consent
3. Women who are S. aureus carriers at the time of recruit.
Exclusion Criteria
2. Women who did not give birth eventually at the Sheba Medical Center.
3. Women who's newborns were not screened at least once during delivery hospitalization.
Enrollment:
300 consecutive women who are defined as S. aureus carriers (see definitions below).
24 Hours
5 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
The Israel Science Foundation
UNKNOWN
Sheba Medical Center
OTHER_GOV
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Gili Regev-Yochay MD
Director, Infection Control Unit
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Dror Charats, Prof.
Role: STUDY_CHAIR
IRB Committee.Sheba Medical Center Israel
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Sheba Medical Center
Ramat Gan, Israel, Israel
Countries
Review the countries where the study has at least one active or historical site.
Central Contacts
Reach out to these primary contacts for questions about participation or study logistics.
Facility Contacts
Find local site contact details for specific facilities participating in the trial.
Gili Regev-Yochay
Role: primary
References
Explore related publications, articles, or registry entries linked to this study.
Leshem E, Maayan-Metzger A, Rahav G, Dolitzki M, Kuint J, Roytman Y, Goral A, Novikov I, Fluss R, Keller N, Regev-Yochay G. Transmission of Staphylococcus aureus from mothers to newborns. Pediatr Infect Dis J. 2012 Apr;31(4):360-3. doi: 10.1097/INF.0b013e318244020e.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
5534-08
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.