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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT04831840
Other study ID # 20201198
Secondary ID
Status Terminated
Phase
First received
Last updated
Start date May 26, 2021
Est. completion date November 20, 2023

Study information

Verified date May 2024
Source University of Miami
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The primary objective is to determine if polymerase chain reaction (PCR) (UTIP™) is more sensitive in identifying urinary tract infections (UTI's) than standard urine cultures.


Recruitment information / eligibility

Status Terminated
Enrollment 32
Est. completion date November 20, 2023
Est. primary completion date November 20, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years to 90 Years
Eligibility Inclusion Criteria: - 18 y/o-90 y/o - Able to consent - Female - Group A only: Recurrent UTI (2 UTIs in 6 months) - Group B only: No history of recurrent UTIs Exclusion Criteria: - Pregnant - Pelvic radiation - Urinary retention (>200 ml residual) - Greater than Stage 2 prolapse - Renal calculi - Immunosuppressed - Neurologic disorder with significant bladder impairment - No current UTI via dip stick

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
United States Holy Cross Hospital Fort Lauderdale Florida
United States University of Miami Miami Florida

Sponsors (1)

Lead Sponsor Collaborator
University of Miami

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Proportion of uropathogens The proportion of uropathogens found on PCR versus urine culture from urine samples. Day 1
Primary Proportion of patients negative for repeat testing The proportion of negative patient on repeat testing of urine samples. Up to 4 weeks
See also
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