Primary Research Questions: Efficacy, safety and feasibility of a 3-month course of levofloxacin in a pilot study will be assessed. 1. Under efficacy, this pilot will determine whether levofloxacin can decrease the incidence of BK viruria and peak urine BK viral load. 2. Under safety, this pilot will determine the incidence of adverse events with levofloxacin. 3. Under feasibility, this pilot will determine the number of kidney transplant patients randomized over an eight month enrolment period, adherence to the levofloxacin and frequency of patient drop-out and loss to follow-up
BK virus infection has emerged as a major complication in renal transplantation leading to a significant reduction in graft survival. There are currently no proven strategies to prevent or treat BK virus infection. Quinolone antibiotics, such as levofloxacin, have demonstrated activity against BK virus. The investigators hypothesize that administration of a quinolone antibiotic, when given early post-transplantation, will prevent the establishment of BK viral replication in the urine and thus prevent systemic BK virus infection. A non-randomized study in kidney transplant recipients found that patients given levofloxacin or ciprofloxacin had a significantly lower incidence of BK viremia compared to those not receiving a quinolone (4% versus 24.5%, P=0.02). Objective: The primary objective of the full trial will be to determine if the quinolone levofloxacin decreases the occurrence of doubling creatinine, transplant failure or death in kidney transplant recipients. The aim of this pilot trial is to assess the efficacy, safety and feasibility of a 3-month course of levofloxacin in the kidney transplant population. Results from this pilot study will provide vital information to design and conduct a large, multi-centre trial to determine if quinolone therapy decreases meaningful clinical outcomes in kidney transplantation. If levofloxacin significantly reduces BK viruria and urine viral loads in kidney transplantation it will provide important justification of biologic effect to progress to the larger trial. If the full trial shows that levofloxacin significantly reduces BK infection and improves outcomes, its use in renal transplantation will be strongly endorsed given the lack of proven therapies for this condition.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
QUADRUPLE
Enrollment
154
500mg, PO, once daily for 3 months
Capital Health - University of Alberta Hospital
Edmonton, Alberta, Canada
Vancouver General Hospital
Vancouver, British Columbia, Canada
St. Paul's Hospital
Vancouver, British Columbia, Canada
Winnipeg Health Science Center
Winnipeg, Manitoba, Canada
QEII Health Science Center
Halifax, Nova Scotia, Canada
St. Joseph's Healthcare
Hamilton, Ontario, Canada
London Health Science Center
London, Ontario, Canada
The Ottawa Hospital
Ottawa, Ontario, Canada
University Health Network
Toronto, Ontario, Canada
St. Michael's Hospital
Toronto, Ontario, Canada
...and 1 more locations
Occurrence of BK Viruria
BK viruria was defined as 500 copies/mL or more of BK virus DNA in the urine.
Time frame: 12 months post-transplantation
Adverse Events
Incidence and type of all adverse events
Time frame: 12 months
Acute Rejection
Incidence of Acute rejection
Time frame: 12 months
Clostridium Difficile Associated Diarrhea
Incidence of microbiologically confirmed clostridium difficile associated diarrhea
Time frame: 12 months
Infections
Incidence of other infections (viral, bacterial and fungal) based on established guidelines
Time frame: 12 months
Quinolone Resistance
Incidence of quinolone resistance where a quinolone would have been a therapeutic option
Time frame: 12 months
Allograft Loss
Absence of kidney function in allograft
Time frame: 12 months
Mortality
Time frame: 12 months
Adherence
Proportion of randomized participants who are adherent to the protocol.
Time frame: 12 months
Use of Quinolones
Use of quinolones outside of the protocol
Time frame: 12 months
Proportion of Patient Drop-out and Loss to Follow-up
Time frame: 12 months
Quantitative BK Urine Viral Load
Time frame: 12 months
BK Viremia
BK viremia defined as ≥250 copies/mL of BK virus DNA in the plasma
Time frame: 12 months
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