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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT01138566
Other study ID # IISP37925
Secondary ID
Status Not yet recruiting
Phase N/A
First received June 4, 2010
Last updated June 4, 2010

Study information

Verified date April 2010
Source Taipei Veterans General Hospital, Taiwan
Contact Chang-Phone Fung, M.D.
Phone +886-2-2875-7494
Email cpfung@vghtpe.gov.tw
Is FDA regulated No
Health authority Taiwan: Department of Health
Study type Observational

Clinical Trial Summary

The purposes of this study are:

1. To estimate the prevalence of extended spectrum β-lactamase (ESBL) and/or AmpC among Enterobacteriaceae which cause community-onset urinary tract infections (UTIs)

2. To collect the background, risk factors and clinical outcome of patients with community-acquired uropathogenic condition related to Enterobacteriaceae (both ESBL, AmpC- and non ESBL and/or AmpC producing) after receive different antibiotic regimens.

3. To develop a scoring system to early identify patients at risk of being infected with ESBL- and/or AmpC-producing Enterobacteriaceae by comparing the risk factors for community-onset UTIs caused by ESBL- and/or AmpC-positive against non ESBL -and/or AmpC Enterobacteriaceae

4. To demonstrate the efficacy and safety of ertapenem for the empiric treatment of community-onset UTIs in patients at risk for ESBL- and/or AmpC-producing organism.

The study hypothesis (i) Patients infected with community-acquired uropathogenic ESBL- and/or AmpC-producing Enterobacteriaceae who receive regimens other than carbapenems have a worse outcome.

(ii) There are certain risk factors predicting the acquisition of community-onset UTIs caused by ESBL- and/or AmpC-producing Enterobacteriaceae.

(iii) The use of ertapenem is an effective and safe empirical therapy compared with other agents for community-onset UTIs caused by ESBL- and/or AmpC-producing Enterobacteriaceae.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 400
Est. completion date
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Adult patients who admitted to the Taipei Veterans General Hospital with the diagnosis of community-onset UTI caused by Enterobacteriaceae will be eligible for inclusion in this study if hospitalization for parental antimicrobial therapy is required

Exclusion Criteria:

- pregnancy or lactation in women,

- history of serious allergy or intolerance to study drug therapy (patients with a history of mild rash to ß-lactams could be enrolled),

- complete obstruction of the urinary tract,

- peri-nephritic or intrarenal abscess, prostatitis, any rapidly progressive disease or terminal illness,

- immuno-compromising illness or immuno suppression therapy, the need for concomitant antimicrobials in addition to study therapy,

- a baseline pathogen resistant to study drug,

- treatment with a systemic antimicrobial agent for >24 h within 72 h prior to enrolment, or absolute neutrophil count <1000/mm3.

- Men with a history or physical findings suggestive of acute or chronic prostatitis will also excluded.

Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
Taiwan Taipei Vterans General Hospital Taipei

Sponsors (2)

Lead Sponsor Collaborator
Taipei Veterans General Hospital, Taiwan Merck Sharp & Dohme Corp.

Country where clinical trial is conducted

Taiwan, 

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