Status:

UNKNOWN

Efficacy of Intravenous Fosfomycin in the Treatment of Complicated Urinary in Real-life Conditions.

Lead Sponsor:

Fundación Pública Andaluza para la gestión de la Investigación en Sevilla

Conditions:

Complicated Urinary Tract Infection

Eligibility:

All Genders

18+ years

Brief Summary

This will be a prospective observational multicentre study in real-life conditions of patients with complicated urinary infection of community presentation caused by Escherichia coli using intravenous...

Detailed Description

The objectives are: 1. To asses the clinical and microbiological efficacy and safety of intravenous fosfomycin in the treatment of complicated urinary tract infections due to Escherichia coli in real...

Eligibility Criteria

Inclusion

  • Fosfomycin cohort:
  • Inclusion criteria: Patients over 18 years of age. Patients who have started treatment with intravenous fosfomycin, estimated that they will require at least 2 days of treatment with fosfomycin, initiated as either as empirical treatment (within 24 hours after the emergency visit or onset of symptoms) or targeted treatment (within 24 hours of the availability of the antibiogram).
  • Exclusion criteria: Patients under 18 years of age. Patients in palliative treatment.
  • Control cohort (objective 1):
  • Inclusion criteria:Patients over 18 years of age. Patients who have started treatment with intravenous quinolones or beta-lactams, estimated that they will require at least 2 days of treatment with the drug, initiated as either as empirical treatment (within 24 hours after the emergency visit or onset of symptoms) or targeted treatment (within 24 hours of the availability of the antibiogram). Each patient from the fosfomycin cohort will be matched with a patient from this control cohort according to their.
  • Exclusion criteria: Patients under 18 years of age.Patients in palliative treatment; Informed consent not signed by the patient.

Exclusion

    Key Trial Info

    Start Date :

    October 21 2019

    Trial Type :

    OBSERVATIONAL

    Allocation :

    ESTIMATED

    End Date :

    December 31 2021

    Estimated Enrollment :

    400 Patients enrolled

    Trial Details

    Trial ID

    NCT04076436

    Start Date

    October 21 2019

    End Date

    December 31 2021

    Last Update

    November 14 2019

    Active Locations (2)

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    Page 1 of 1 (2 locations)

    1

    Hospital Universitario Reina Sofía

    Córdoba, Spain, 14004

    2

    Hospital Universitario Virgen Macarena

    Seville, Spain, 41009