- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01125384
Comparison Between Two Methods of Throat Swabbing
August 27, 2011 updated by: Meir Medical Center
Throat swabbing is an important instrument in the diagnosis of strep pharyngitis and sometimes the main argument for antibiotic treatment.
There is no firm knowledge about an appropriate method of the swabbing for receiving maximal sensitivity.
We hypothesize that accurate swabbing from the pus will increase the sensitivity of the swabbing as compared to free swabbing.
In order to check this hypothesis we will compare two swabs from the same throat.
One that will be taken by a physician specifically from the pass and the second will be taken by a nurse as she used to do it.
An increase of 10% of positive results will be accepted as a significant advantage.
Study Overview
Study Type
Interventional
Enrollment (Anticipated)
500
Phase
- Not Applicable
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 45 years (Child, Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- patients with sore throat, classified 2-3 according to Cantor's criteria
Exclusion Criteria:
- patients on antibiotic treatment
- suspected carriers of streptococcus
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
- Primary Purpose: Diagnostic
- Allocation: Non-Randomized
- Interventional Model: Single Group Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
No Intervention: nurse swabbing
|
|
|
Experimental: "accurate" swabbing by a physician
|
physician swabs patient's throat according to standard rules before referral of the patient to throat swabbing by nurse.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
sensitivity of "accurate" swabbing versus sensitivity of habitual nurses' swabbing
Time Frame: 1 year
|
Proportion of positive cultures obtained by "accurate" swabbing will be compared to the proportion of positive cultures obtained by nurses' habitual swabbing (as they do it usually).
|
1 year
|
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
May 1, 2010
Primary Completion (Actual)
June 1, 2011
Study Completion (Actual)
June 1, 2011
Study Registration Dates
First Submitted
May 2, 2010
First Submitted That Met QC Criteria
May 17, 2010
First Posted (Estimate)
May 18, 2010
Study Record Updates
Last Update Posted (Estimate)
August 30, 2011
Last Update Submitted That Met QC Criteria
August 27, 2011
Last Verified
August 1, 2011
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- MMC10104-09CTIL
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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