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Quinolone Prophylaxis for the Prevention of BK Virus Infection in Kidney Transplantation: A Pilot Study

Primary Purpose

Disease Due to BK Polyomavirus, Kidney Transplant Infection

Status
Completed
Phase
Phase 4
Locations
Canada
Study Type
Interventional
Intervention
Levofloxacin
Sponsored by
Ottawa Hospital Research Institute
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Disease Due to BK Polyomavirus focused on measuring Kidney Transplant, BK Polyomavirus Infection

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • a primary or repeat kidney transplant recipient (deceased or living donor)
  • age greater or equal to 18 years

Exclusion Criteria:

  • Unable to provide informed consent
  • Greater than 5 days post-transplantation
  • BK virus nephropathy with a previous transplant
  • History of allergic reaction to any quinolone antibiotic
  • History of quinolone associated tendonitis or tendon rupture
  • Corrected QT interval prolongation on EKG as defined by Al-Khatib
  • Concomitant use of medication known to prolong the QT interval such as class IA antiarrhythmic drugs (e.g. quinidine, procainamide, disopyramide), class III antiarrhythmic drugs (e.g. amiodarone, sotalol), azole antifungals (e.g. fluconazole) or macrolide antibiotics (e.g. erythromycin)
  • Pregnant or breastfeeding as safety of levofloxacin not established
  • Requires quinolone antibiotic for more than 14 days (e.g. for UTI prophylaxis)
  • Recipient of a multi-organ transplant (e.g. kidney-pancreas)
  • Currently enrolled in another interventional trial
  • Previously enrolled in this study
  • History of rhabdomyolysis
  • Significant allergic reaction to ≥ 3 classes of antibiotics as these patients may have no other option other than quinolones for routine infection.

Sites / Locations

  • Capital Health - University of Alberta Hospital
  • Vancouver General Hospital
  • St. Paul's Hospital
  • Winnipeg Health Science Center
  • QEII Health Science Center
  • St. Joseph's Healthcare
  • London Health Science Center
  • The Ottawa Hospital
  • University Health Network
  • St. Michael's Hospital
  • McGill University Health Center

Arms of the Study

Arm 1

Arm 2

Arm Type

Placebo Comparator

Active Comparator

Arm Label

sugar pill

levofloxacin

Arm Description

Outcomes

Primary Outcome Measures

Efficacy: The time to occurence of BK viruria
BK viruria will be defined as ≥1000 copies/mL ok BK virus DNA in the urine.

Secondary Outcome Measures

Adverse Events
Incidence and type of all adverse events
Acute rejection
Incidence of Acute rejection
Clostridium difficile associated diarrhea
Incidence of microbiologically confirmed clostridium difficile associated diarrhea
Infections
Incidence of other infections (viral, bacterial and fungal) based on established guidelines
Quinolone resistance
Incidence of quinolone resistance where a quinolone would have been a therapeutic option
Effect of levofloxacin on immunosuppressive drug doses and blood levels
Transplant failure
Mortality
Number of patients transplanted
Number of patients transplanted during the 8 month recruitment period who are randomized into the trial
Adherence
Proportion of randomized participants who are adherent to the protocol.
Use of quinolones
Use of quinolones outside of the protocol
Proportion of patient drop-out and loss to follow-up
Quantitative BK urine viral load
BK viremia
Time to occurence of BK viremia, defined as ≥250 copies/mL of BK virus DNA in the plasma

Full Information

First Posted
May 11, 2011
Last Updated
October 14, 2014
Sponsor
Ottawa Hospital Research Institute
Collaborators
Canadian Institutes of Health Research (CIHR), St. Paul's Hospital, Canada, Vancouver General Hospital, University of Alberta, University of Manitoba, University Health Network, Toronto, Unity Health Toronto, St. Joseph's Healthcare Hamilton, London Health Sciences Centre, McGill University Health Centre/Research Institute of the McGill University Health Centre, Dalhousie University
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1. Study Identification

Unique Protocol Identification Number
NCT01353339
Brief Title
Quinolone Prophylaxis for the Prevention of BK Virus Infection in Kidney Transplantation: A Pilot Study
Official Title
Quinolone Prophylaxis for the Prevention of BK Virus Infection in Kidney Transplantation: A Pilot Study
Study Type
Interventional

2. Study Status

Record Verification Date
October 2014
Overall Recruitment Status
Completed
Study Start Date
November 2011 (undefined)
Primary Completion Date
April 2014 (Actual)
Study Completion Date
October 2014 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Ottawa Hospital Research Institute
Collaborators
Canadian Institutes of Health Research (CIHR), St. Paul's Hospital, Canada, Vancouver General Hospital, University of Alberta, University of Manitoba, University Health Network, Toronto, Unity Health Toronto, St. Joseph's Healthcare Hamilton, London Health Sciences Centre, McGill University Health Centre/Research Institute of the McGill University Health Centre, Dalhousie University

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Primary Research Questions: Efficacy, safety and feasibility of a 3-month course of levofloxacin in a pilot study will be assessed. Under efficacy, this pilot will determine whether levofloxacin can decrease the incidence of BK viruria and peak urine BK viral load. Under safety, this pilot will determine the incidence of adverse events with levofloxacin. 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
Detailed Description
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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Disease Due to BK Polyomavirus, Kidney Transplant Infection
Keywords
Kidney Transplant, BK Polyomavirus Infection

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
154 (Actual)

8. Arms, Groups, and Interventions

Arm Title
sugar pill
Arm Type
Placebo Comparator
Arm Title
levofloxacin
Arm Type
Active Comparator
Intervention Type
Drug
Intervention Name(s)
Levofloxacin
Other Intervention Name(s)
Apo-levofloxacin, DIN 02284707
Intervention Description
500mg, PO, once daily for 3 months
Primary Outcome Measure Information:
Title
Efficacy: The time to occurence of BK viruria
Description
BK viruria will be defined as ≥1000 copies/mL ok BK virus DNA in the urine.
Time Frame
12 months post-transplantation
Secondary Outcome Measure Information:
Title
Adverse Events
Description
Incidence and type of all adverse events
Time Frame
12 months
Title
Acute rejection
Description
Incidence of Acute rejection
Time Frame
12 months
Title
Clostridium difficile associated diarrhea
Description
Incidence of microbiologically confirmed clostridium difficile associated diarrhea
Time Frame
12 months
Title
Infections
Description
Incidence of other infections (viral, bacterial and fungal) based on established guidelines
Time Frame
12 months
Title
Quinolone resistance
Description
Incidence of quinolone resistance where a quinolone would have been a therapeutic option
Time Frame
12 months
Title
Effect of levofloxacin on immunosuppressive drug doses and blood levels
Time Frame
12 months
Title
Transplant failure
Time Frame
12 months
Title
Mortality
Time Frame
12 months
Title
Number of patients transplanted
Description
Number of patients transplanted during the 8 month recruitment period who are randomized into the trial
Time Frame
12 months
Title
Adherence
Description
Proportion of randomized participants who are adherent to the protocol.
Time Frame
12 months
Title
Use of quinolones
Description
Use of quinolones outside of the protocol
Time Frame
12 months
Title
Proportion of patient drop-out and loss to follow-up
Time Frame
12 months
Title
Quantitative BK urine viral load
Time Frame
12 months
Title
BK viremia
Description
Time to occurence of BK viremia, defined as ≥250 copies/mL of BK virus DNA in the plasma
Time Frame
12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: a primary or repeat kidney transplant recipient (deceased or living donor) age greater or equal to 18 years Exclusion Criteria: Unable to provide informed consent Greater than 5 days post-transplantation BK virus nephropathy with a previous transplant History of allergic reaction to any quinolone antibiotic History of quinolone associated tendonitis or tendon rupture Corrected QT interval prolongation on EKG as defined by Al-Khatib Concomitant use of medication known to prolong the QT interval such as class IA antiarrhythmic drugs (e.g. quinidine, procainamide, disopyramide), class III antiarrhythmic drugs (e.g. amiodarone, sotalol), azole antifungals (e.g. fluconazole) or macrolide antibiotics (e.g. erythromycin) Pregnant or breastfeeding as safety of levofloxacin not established Requires quinolone antibiotic for more than 14 days (e.g. for UTI prophylaxis) Recipient of a multi-organ transplant (e.g. kidney-pancreas) Currently enrolled in another interventional trial Previously enrolled in this study History of rhabdomyolysis Significant allergic reaction to ≥ 3 classes of antibiotics as these patients may have no other option other than quinolones for routine infection.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Greg Knoll, MD
Organizational Affiliation
Ottawa Hospital Research Institute
Official's Role
Principal Investigator
Facility Information:
Facility Name
Capital Health - University of Alberta Hospital
City
Edmonton
State/Province
Alberta
ZIP/Postal Code
T6G 2B7
Country
Canada
Facility Name
Vancouver General Hospital
City
Vancouver
State/Province
British Columbia
ZIP/Postal Code
V5Z 1M9
Country
Canada
Facility Name
St. Paul's Hospital
City
Vancouver
State/Province
British Columbia
ZIP/Postal Code
V6Z 1Y6
Country
Canada
Facility Name
Winnipeg Health Science Center
City
Winnipeg
State/Province
Manitoba
Country
Canada
Facility Name
QEII Health Science Center
City
Halifax
State/Province
Nova Scotia
Country
Canada
Facility Name
St. Joseph's Healthcare
City
Hamilton
State/Province
Ontario
ZIP/Postal Code
L8N 4A6
Country
Canada
Facility Name
London Health Science Center
City
London
State/Province
Ontario
ZIP/Postal Code
N6A 5A5
Country
Canada
Facility Name
The Ottawa Hospital
City
Ottawa
State/Province
Ontario
ZIP/Postal Code
K1H 8L6
Country
Canada
Facility Name
University Health Network
City
Toronto
State/Province
Ontario
ZIP/Postal Code
M5G 2N2
Country
Canada
Facility Name
St. Michael's Hospital
City
Toronto
State/Province
Ontario
Country
Canada
Facility Name
McGill University Health Center
City
Montreal
State/Province
Quebec
ZIP/Postal Code
H3A 1A1
Country
Canada

12. IPD Sharing Statement

Citations:
PubMed Identifier
25399012
Citation
Knoll GA, Humar A, Fergusson D, Johnston O, House AA, Kim SJ, Ramsay T, Chasse M, Pang X, Zaltzman J, Cockfield S, Cantarovich M, Karpinski M, Lebel L, Gill JS. Levofloxacin for BK virus prophylaxis following kidney transplantation: a randomized clinical trial. JAMA. 2014 Nov 26;312(20):2106-14. doi: 10.1001/jama.2014.14721.
Results Reference
derived
PubMed Identifier
23800312
Citation
Humar A, Gill J, Johnston O, Fergusson D, House AA, Lebel L, Cockfield S, Kim SJ, Zaltzman J, Cantarovich M, Karpinski M, Ramsay T, Knoll GA. Quinolone prophylaxis for the prevention of BK virus infection in kidney transplantation: study protocol for a randomized controlled trial. Trials. 2013 Jun 21;14:185. doi: 10.1186/1745-6215-14-185.
Results Reference
derived

Learn more about this trial

Quinolone Prophylaxis for the Prevention of BK Virus Infection in Kidney Transplantation: A Pilot Study

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