- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02972437
Detection of Group A Streptococcus (GAS) in Oral Cavity
November 27, 2016 updated by: Hadassah Medical Organization
Detection of Group A Streptococcus (GAS) in Oral Cavity Using Molecular Techniques
The investigators intend to screen children who are suspected of having GAS tonsillitis.
From each child we will take a throat culture and saliva sample to screen for molecular evidence of GAS.
Study Overview
Study Type
Observational
Enrollment (Anticipated)
100
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: saar hashavya, doctor
- Phone Number: 972 53 223 3987
- Email: saarha@gmail.com
Study Contact Backup
- Name: naama shwartz, doctor
- Phone Number: 972545216158
- Email: naamapines@gmail.com
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
3 years to 16 years (Child)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
children 3-16 years old with evidence of tonsilitis
Description
Inclusion Criteria:
- clinical evidence of GAS tonsillitis
- healthy, no chronic illness
- not a GAS carrier
Exclusion Criteria:
- GAS carrier
- Active background disease
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
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
molecular detection of GAS compared to throat culture detection
Time Frame: 3 days
|
3 days after taking the oral sample, the investigators will compare it to the throat culture taken at the same time.
|
3 days
|
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 Major Dates
Study Start
December 1, 2016
Primary Completion (Anticipated)
December 1, 2017
Study Completion (Anticipated)
January 1, 2018
Study Registration Dates
First Submitted
November 16, 2016
First Submitted That Met QC Criteria
November 21, 2016
First Posted (Estimate)
November 23, 2016
Study Record Updates
Last Update Posted (Estimate)
November 29, 2016
Last Update Submitted That Met QC Criteria
November 27, 2016
Last Verified
November 1, 2016
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- naamap-HMO-CTIL
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
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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