Strep A FIA Field Study, Sofia
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The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. |
| ClinicalTrials.gov Identifier: NCT02153008 |
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Recruitment Status :
Completed
First Posted : June 2, 2014
Last Update Posted : August 3, 2017
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| Condition or disease |
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| Group A Streptococcus |
| Study Type : | Observational |
| Actual Enrollment : | 1708 participants |
| Observational Model: | Other |
| Time Perspective: | Prospective |
| Official Title: | Sofia Strep A FIA Field Study |
| Actual Study Start Date : | April 2014 |
| Actual Primary Completion Date : | July 1, 2016 |
| Actual Study Completion Date : | July 1, 2016 |
| Group/Cohort |
|---|
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Symptomatic population for GAS
This study is a diagnostic study to aid in the detection of Strep throat. No intervention or medication is a part of this study.
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- Detection of Group A Streptococcus [ Time Frame: Within 5 minutes ]A throat swab specimen will be obtained and tested for the presence of Group A Streptococcus via the Sofia Analyzer
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.
| Ages Eligible for Study: | 3 Years and older (Child, Adult, Older Adult) |
| Sexes Eligible for Study: | All |
| Accepts Healthy Volunteers: | No |
| Sampling Method: | Non-Probability Sample |
Inclusion Criteria:
- Male and Female, 3 years of age or older
- Must currently be exhibiting one or more of the symptoms characteristic of pharyngitis to be eligible for inclusion in this study.
For example:
- Acute onset of sore throat
- Redness of the posterior pharyngeal wall
- Difficulty/pain on swallowing
- Fever, > 37.8º C (100ºF) at presentation or within past 24 hours
- Pharyngeal exudate
- Tender cervical lymphadenopathy
- Absence of cough, runny nose or other upper respiratory symptoms.*
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Other, symptoms specific to Strep A not listed above.
- Must include at least one additional symptom from a-f and cannot be the only criteria used to meet inclusion for enrollment in the study.
Exclusion Criteria:
- Subjects currently under treatment with antibiotics are not to be included in this study.
- At clinical sites requiring informed consent, unable to understand and consent to participation; for minors this includes parent or legal guardian.
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02153008
| United States, Arizona | |
| Best Medical Group, LLC | |
| Phoenix, Arizona, United States, 85042-6510 | |
| United States, Florida | |
| Gentle Medical Associates | |
| Boynton Beach, Florida, United States, 33435 | |
| Pediatrics by the Sea | |
| Delray Beach, Florida, United States, 33483 | |
| Teena Hughes, MD | |
| Tampa, Florida, United States, 33613 | |
| United States, New York | |
| Twelve Corners Pediatrics | |
| Rochester, New York, United States, 14618 | |
| United States, Texas | |
| Veritas, PA | |
| Belton, Texas, United States, 76513 | |
| United States, Virginia | |
| Advanced Pediatrics | |
| Vienna, Virginia, United States, 22180 | |
| Study Director: | John D. Tamerius, PhD | Quidel Corporation |
| Responsible Party: | Quidel Corporation |
| ClinicalTrials.gov Identifier: | NCT02153008 |
| Other Study ID Numbers: |
CS-0142-07 |
| First Posted: | June 2, 2014 Key Record Dates |
| Last Update Posted: | August 3, 2017 |
| Last Verified: | August 2017 |
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Strep throat |

