Ignite Creation Date:
2024-05-06 @ 7:55 AM
Last Modification Date:
2024-10-26 @ 11:53 AM
Study NCT ID:
NCT02623179
Status:
COMPLETED
Last Update Posted:
2017-10-05
First Post:
2015-12-01
Brief Title:
Conventional and Molecular Diagnostic Method for Patients With Suspected UTI
Sponsor:
Southwest Regional PCR LLC
Organization:
Southwest Regional PCR LLC
Study Overview
Official Title:
Conventional and Molecular Diagnostic Method for Patients With Suspected Urinary Tract Infections Clinical Economic and Quality of Life Outcomes
Status:
COMPLETED
Status Verified Date:
2017-10
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
In this protocol the investigators are examining the use of a novel pathogen testing technology and method of identification of antibiotic susceptibility against the conventional C S testing for patients with both complicated and uncomplicated UTIs The investigators will examine the two modes in terms of objective patient related outcomes ie 1 diagnostic accuracy and degree of detail of final analysis 2 time to resolution of symptoms 3 quality of life as defined by particularly symptomology and bothersomeness of the symptoms and 4 overall cost
Detailed Description:
None
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None