Ignite Creation Date:
2024-05-06 @ 9:53 AM
Last Modification Date:
2024-10-26 @ 12:21 PM
Study NCT ID:
NCT03098394
Status:
TERMINATED
Last Update Posted:
2023-08-31
First Post:
2017-03-27
Brief Title:
Use of a Rapid Test for Gonorrhea Chlamydia for Women Presenting With Possible Sexually Transmitted Infections
Sponsor:
University of Maryland Baltimore
Organization:
University of Maryland Baltimore
Study Overview
Official Title:
Use of a Rapid Turnaround Test for Gonorrhea Chlamydia to Improve Treatment of Women Presenting With Possible Sexually Transmitted Infections
Status:
TERMINATED
Status Verified Date:
2023-08
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Low enrollment
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
The purpose of this study is to evaluate the effect of utilizing a rapid turnaround CTNG test on treatment of female patients in the emergency department or urgent care setting with possible STIs
Detailed Description:
All females ages 18-55 presenting to the University of Maryland Medical Center Emergency Department or Urgent Care whose provider suspects sexually transmitted infection will be offered study enrollment and be randomly assigned to either the control or the experimental group Both groups will have a urinalysis a pregnancy test a pelvic exam and an endocervical sample collected but the experimental groups urine will be used to run the rapid turnaround test RTAT instead of the standard PCR Data will be collected regarding provider decision making length of stay in the emergency department patient satisfaction clinician satisfaction further healthcare sought by patient and cost surrounding each treatment
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
True
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
True
Is an FDA AA801 Violation?:
None