Efficacy of 7 Days Versus 14 Days of Antibiotic Therapy for Acute Pyelonephritis in Kidney Transplant Recipients, a Multicentre Randomized Non-inferiority Trial.

NCT ID: NCT05597540

Last Updated: 2024-05-29

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

RECRUITING

Clinical Phase

PHASE3

Total Enrollment

470 participants

Study Classification

INTERVENTIONAL

Study Start Date

2024-02-22

Study Completion Date

2027-08-22

Brief Summary

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Infections are a major cause of morbidity and mortality in solid organ transplant recipients. In kidney transplant recipients (KTR) urinary tract infection (UTI) represent 45-72% of all infections, and 30% of all hospitalizations for sepsis. Acute transplant pyelonephritis are the most common complications occurring in more than 20% of patients, mainly in the first year after transplantation. They are associated with an increased risk of acute kidney rejection and long-term kidney graft dysfunction. Gram-negative bacteria, mainly E. coli, account for more than 70% of UTI in KTR. As those infections are favoured by urinary tract modifications/defects and immunosuppression, they are often recurrent and necessitate repeated courses of antibiotics. Selective pressure due to antibiotic consumption, along with frequent hospital admissions and immunosuppression, are well known risk factors for the development of antibiotic resistant infections. Multidrug (MDR)- or extensively (XDR)- drug resistant Enterobacteriaceae including ESBL- or carbapenemase-producing organisms, are thus increasingly observed in transplant units and represent a global threat as very few new antibiotics are expected in the next decade.

One main strategy to limit antimicrobial resistance is to reduce the duration of antibiotic treatment. A 7 day-course is recommended for simple acute pyelonephritis (APN) treated with fluoroquinolones or parenteral B-lactams, prolonged up to 10 or 14 days in the presence of underlying disease at risk of complications. Most KT teams treat patients between 14-21 days as recommended by American guidelines. However, the need to extend treatment duration in immunosuppressed patients is a poorly defined concept and the optimal duration of treatment for APN in KTR is not known as these patients are excluded from most studies.

As there is an urgent need to reduce antibiotic consumption in this population at high risk of developing infections due to resistant pathogens, the hypothesis is that a 7 day-treatment is sufficient to cure APN with good clinical response after 48h of treatment in KTR and is as effective as 14 days.

Detailed Description

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Conditions

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Pyelonephritis Acute Kidney Transplant Infection

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Outcome Assessors
Randomized double blind trial

Study Groups

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7 day-duration antibiotic treatment

Group Type EXPERIMENTAL

Short antibiotic treatment

Intervention Type DRUG

7 day-duration antibiotic treatment. The choice of antibiotic treatment is left to the medical team in charge of the patient.

14 day-duration antibiotic treatment

Group Type ACTIVE_COMPARATOR

Usual antibiotic treatment

Intervention Type DRUG

14 day-duration antibiotic treatment. The choice of antibiotic treatment is left to the medical team in charge of the patient.

Interventions

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Short antibiotic treatment

7 day-duration antibiotic treatment. The choice of antibiotic treatment is left to the medical team in charge of the patient.

Intervention Type DRUG

Usual antibiotic treatment

14 day-duration antibiotic treatment. The choice of antibiotic treatment is left to the medical team in charge of the patient.

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

* Age \>18 years KTR
* APN defined by: fever (T°≥38°C) (with or without clinical signs and/or symptoms of UTI) and pyuria (≥10\^4 white blood cells/mL or ≥10/mm3) and positive urine culture (uropathogen ≥10\^3 CFU/mL susceptible to the empirically administrated antibiotic)
* No confirmed or suspected febrile non urinary bacterial infection
* No urologic/renal complication at baseline imaging (abscess, obstruction...)
* Favourable early response to antibiotic treatment:48 to 60 hours after the first dose of antibiotic effective against the causative uropathogen) defined by: T°\<38°C and improvement (or resolution) of signs and/or symptoms of urinary tract infection if present at diagnosis
* Written informed consent

Exclusion Criteria

* Severe or complicated condition

* Any rapidly progressing disease or immediately life-threatening illness, including, but not limited to, septic shock, current or impeding respiratory failure, acute heart or liver failure
* Admission or stay in intensive care unit at baseline
* Obstruction of the urinary tract
* Renal, perinephric or prostatic abscess
* Prior inclusion in this study
* Current participation to another interventional study
* Dual antibiotic therapy (prophylactic antibiotic such as cotrimoxazole allowed) (only 1 dose of aminoside is allowed before randomization)
* First month post transplantation
* Current indwelling catheter (including bladder catheter, ureteral stents, percutaneous nephrostomy tubes)
* Neurogenic bladder
* Enterocystoplasty
* Immunodeficiency or immunosuppressive therapy not related to kidney transplantation including hematologic malignancy, cancer, asplenia, neutropenia\<500 neutrophils/mm3
* Pregnancy, breastfeeding
* Hypersensitivity or previous severe adverse drug reaction to the antibiotic therapy
* Unable or unwilling, in the judgment of the investigator, to comply with the protocol
* Life expectancy\<1 month
* Patient under legal guardianship or without healthcare coverage
* Homeless patient
* Women with childbearing potential not using adequate contraception
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Assistance Publique - Hôpitaux de Paris

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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CHU Bordeaux

Bordeaux, , France

Site Status NOT_YET_RECRUITING

Hôpital Foch

Boulogne-Billancourt, , France

Site Status NOT_YET_RECRUITING

CHU Mondor

Créteil, , France

Site Status RECRUITING

CHU Lyon

Lyon, , France

Site Status NOT_YET_RECRUITING

CHU Nantes

Nantes, , France

Site Status RECRUITING

CHU Kremlin-Bicêtre

Paris, , France

Site Status NOT_YET_RECRUITING

CHU Necker

Paris, , France

Site Status RECRUITING

CHU Saint Louis

Paris, , France

Site Status RECRUITING

CHU Toulouse

Toulouse, , France

Site Status NOT_YET_RECRUITING

Countries

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France

Central Contacts

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Matthieu Lafaurie, MD

Role: CONTACT

142494117 ext. +33

Jérôme Lambert, Pr

Role: CONTACT

142499742 ext. +33

Facility Contacts

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Hannah Kaminski, Dr

Role: primary

Michel Delahousse, Dr

Role: primary

Marie Matignon, Dr

Role: primary

Charlene Levi, Dr

Role: primary

Clément Deltombe, Dr

Role: primary

Renaud Snanoudj, Pr

Role: primary

Carole Burger, Dr

Role: primary

Gillian Divard, Dr

Role: primary

Nassim Kamar, Pr

Role: primary

Other Identifiers

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APHP200020

Identifier Type: -

Identifier Source: org_study_id

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