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Recurrent Urinary Tract Infections and the Microbiome

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University of Miami

Status

Terminated

Conditions

Recurrent Urinary Tract Infection

Study type

Observational

Funder types

Other

Identifiers

NCT04831840
20201198

Details and patient eligibility

About

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.

Enrollment

32 patients

Sex

Female

Ages

18 to 90 years old

Volunteers

Accepts Healthy Volunteers

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

Trial design

32 participants in 2 patient groups

Female participants with recurrent urinary tract infections (RUTI).
Description:
Patients with RUTIs (Group A) will provide two urine samples. One urine sample is a clean catch and the other is a catheterized specimen. Both will be sent for analysis. A perineal swab will also be collect and analyzed for each patient.
Female control patients without RUTIs
Description:
Patients without RUTIs (Group B) will provide two urine samples. One urine sample is a clean catch and the other is a catheterized specimen. Both will be sent for analysis. A perineal swab will also be collect and analyzed for each patient.

Trial contacts and locations

2

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Central trial contact

Laura Martin, DO

Data sourced from clinicaltrials.gov

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