Clinical Utility of Rapid CT/NG Testing in the ED
Last updated on April 2022Recruitment
- Recruitment Status
- Completed
Inclusion Criteria
- The study population includes women between the age of 18 and 50 who present to the ED and are going to receive CT/NG testing in the ED.
- The study population includes women between the age of 18 and 50 who present to the ED and are going to receive CT/NG testing in the ED.
Exclusion Criteria
- Patients will be excluded if they are unable to provide informed consent or are not English speaking.
- Patients will be excluded if they are unable to provide informed consent or are not English speaking.
Summary
- Conditions
- Sexually Transmitted Diseases
- Type
- Interventional
- Design
- Allocation: Randomized
- Intervention Model: Parallel Assignment
- Masking: None (Open Label)
Participation Requirements
- Age
- Between 18 years and 50 years
- Gender
- Only females
Inclusion Criteria
- The study population includes women between the age of 18 and 50 who present to the ED and are going to receive CT/NG testing in the ED.
- The study population includes women between the age of 18 and 50 who present to the ED and are going to receive CT/NG testing in the ED.
Exclusion Criteria
- Patients will be excluded if they are unable to provide informed consent or are not English speaking.
- Patients will be excluded if they are unable to provide informed consent or are not English speaking.
Tracking Information
- NCT #
- NCT02200224
- Collaborators
- National Institute for Biomedical Imaging and Bioengineering (NIBIB)
- Investigators
- Principal Investigator: Andrea Dugas, MD,PhD Johns Hopkins University
- Andrea Dugas, MD,PhD Johns Hopkins University
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