Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00195286
Other study ID # 101315
Secondary ID
Status Completed
Phase Phase 4
First received September 12, 2005
Last updated September 24, 2009
Start date June 2004
Est. completion date July 2007

Study information

Verified date September 2009
Source Wyeth is now a wholly owned subsidiary of Pfizer
Contact n/a
Is FDA regulated No
Health authority Spain: Spanish Agency of Medicines
Study type Observational

Clinical Trial Summary

The primary objective is to study the efficacy of piperacillin/tazobactam in patients with complicated urinary tract infections


Recruitment information / eligibility

Status Completed
Enrollment 180
Est. completion date July 2007
Est. primary completion date July 2007
Accepts healthy volunteers No
Gender Both
Age group 16 Years and older
Eligibility Inclusion Criteria:

- Hospitalized patients over 16 years of age with complicated urinary infection produced by bacteria that are suspected to be susceptible to treatment with Piperacillin-tazobactam.

Exclusion Criteria:

- Patients known, or thought to be hypersensitivity to beta-lactams

- Patients with an uncomplicated urinary tract infection

Study Design

Observational Model: Case-Only, Time Perspective: Prospective


Intervention

Drug:
piperacillin/tazobactam


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Wyeth is now a wholly owned subsidiary of Pfizer

Country where clinical trial is conducted

Spain, 

See also
  Status Clinical Trial Phase
Terminated NCT00560924 - Preventive Effect of Treatment With Estradiol Vaginal Tablets on Recurrent Urinary Tract Infections in Post-menopausal Women Phase 3
Recruiting NCT02658903 - Prevention of Catheter Associated Lower Urinary Infections Using the Oxys Indwelling Catheter Phase 1