Status:

COMPLETED

Treatment's Duration of Acute Uncomplicated Pyelonephritis

Lead Sponsor:

Assistance Publique - Hôpitaux de Paris

Conditions:

Urinary Tract Infection

Fever

Eligibility:

FEMALE

18-65 years

Phase:

PHASE4

Brief Summary

The purpose of this study is to compare the efficacy of 5 days versus 10 days treatment duration in uncomplicated acute pyelonephritis. Acute pyelonephritis is a common disease and the treatment dura...

Detailed Description

1. State of the issue and objective of the research The acute pyelonephritis (AP) represent the most frequent COMMUNAUTARY bacterial infection. Currently, usual recommended duration of antibiotherapy ...

Eligibility Criteria

Inclusion

  • Women 18 to 65 years old
  • Non-immunocompromised
  • Conducting a medical examination prior
  • Signature of informed consent in writing.
  • Clinical signs of urinary tract infection (urinary burning, urgency, pollakiuria, dysuria, pyuria, lumbar or pelvic pain),
  • A temperature\> 38 ° C,
  • A positive ECBU direct seed (s) sensitive (s) to the fluoroquinolones

Exclusion

  • Antibiotic therapy prior
  • Presence of complications of PNA (abscesses, dilated excretory pathways, probe urinary bladder, neurological, transplant, kidney single functional or anatomical),
  • An episode of PNA within 6 months,
  • having fluoroquinolones in 6 months,
  • Infection on urinary endo-material (prosthetic urethral, ureteral probe)
  • The immunodepressed (known seropositivity for HIV, asplenia, diabetes neutropenia, agammaglobulinemia ...)
  • Pregnancy and lactation,
  • Allergy to antibiotics,
  • Corticosteroids concomitantly taking fluoroquinolones,
  • History of TENDINOPATHY with a fluoroquinolone
  • History of epilepsy
  • Deficit known as glucose-6-phosphate dehydrogenase
  • Life expectancy \<1 month
  • Cognitive major
  • Patient under guardianship, CURATORSHIP or without coverage,
  • The need for immunosuppressive or corticosteroid therapy,
  • The need for other concomitant antibiotic treatment, whatever the cause
  • No affiliation to a social security scheme (beneficiary or beneficiary).

Key Trial Info

Start Date :

June 1 2009

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

August 1 2011

Estimated Enrollment :

310 Patients enrolled

Trial Details

Trial ID

NCT00873626

Start Date

June 1 2009

End Date

August 1 2011

Last Update

November 6 2014

Active Locations (2)

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Page 1 of 1 (2 locations)

1

University hospital of Garches

Garches, France, 92380

2

university hospital of TOURS

Tours, France