- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00646919
Preoperative Nasal Swabs From Pediatric Patients
March 26, 2008 updated by: Hillel Yaffe Medical Center
Double-Blind Prospective Study Concerning the Connection Between Positive Nasal Culture for Staphyloccoci in Pediatric Patients Undergoing Any Elective Surgery in the Out-Patient Clinic in the Hillel Yaffe Medical Center, Over a Period of One Year
We intend to take a nasal swab from each pediatric pre-operative patient in our out-clinic with the intention of looking for a connection between positive operative incisions and a positive nasal swab.
The patients will be in the out-patient clinic for a few hours, and will be examined post-operatively after one week.
Those with positive nasal swabs will be advised to apply a nasal cream (Mupirocin)in their noses for one week.
Our hypothesis is that there is a correlation between positive nasal swabs and positive incision infections.
Study Overview
Study Type
Observational
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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-
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Hadera, Israel, 38100
- Hillel Yaffe Medical Center
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Contact:
- Gershon Keren, MD
- Phone Number: 972-4-6304218
- Email: gershonk@hy.health.gov.il
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Sub-Investigator:
- Zvi Steiner, MD
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
No older than 16 years (Child)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
All pediatric patients attending our outpatient surgery clinic
Description
Inclusion Criteria:
- All pediatric patients attending outpatient surgery clinic
Exclusion Criteria:
- All others
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
1
All pre-operative pediatric patients in our outpatient clinic
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Registration Dates
First Submitted
March 26, 2008
First Submitted That Met QC Criteria
March 26, 2008
First Posted (Estimate)
March 31, 2008
Study Record Updates
Last Update Posted (Estimate)
March 31, 2008
Last Update Submitted That Met QC Criteria
March 26, 2008
Last Verified
March 1, 2008
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- HY56/2007
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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