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A Trial Assessing Peri-procedure Chemoprophylaxis During Transrectal Prostate Needle Biopsy

Primary Purpose

Benign Prostate Hyperplasia

Status
Completed
Phase
Phase 4
Locations
Egypt
Study Type
Interventional
Intervention
ciprofloxacin
ciprofloxacin and gentamycine
culture based chemoprophylaxis
Sponsored by
Mansoura University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Benign Prostate Hyperplasia focused on measuring Chemoprevention

Eligibility Criteria

undefined - undefined (Child, Adult, Older Adult)MaleDoes not accept healthy volunteers

Inclusion Criteria:

  1. Prothrombin concentration > 70%
  2. Platelet count > 100.000/cm

Exclusion Criteria:

  1. Acute prostatitis (positive symptoms and signs)
  2. Patients with compromised renal function (serum creatinine >1.6 mg/dl)
  3. Uncontrolled DM
  4. Patients on immunosuppressive therapy
  5. Active steroid intake
  6. Untreated bleeding diathesis

Sites / Locations

  • Urology and Nprhology Center

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Active Comparator

Experimental

Experimental

Arm Label

ciprofloxacin

ciprofloxacin and gentamycine

culture based chemoprophylaxis

Arm Description

standard chemoprophylaxis [500mg ciprofloxacin twice daily for 3 days]

Augmented Chemoprophylaxis [standard chemoprophylaxis plus 160mg]

Patients will receive antibiotic according to rectal swab culture at time of biopsy and then after for 3 days.

Outcomes

Primary Outcome Measures

occurrence of post procedure infectious complications
occurrence of post procedure infectious complications (e.g urosepsis and local genital or prostate infectious complications). Sepsis is identified as occurrence of two or more of SIRS criteria.

Secondary Outcome Measures

flouroquinolones resistance in rectal carriage
identification of the prevalence of flouroquinolones resistance in rectal carriage in this subset of patients and post procedure non-infectious complications.
post procedure non-infectious complications

Full Information

First Posted
March 24, 2015
Last Updated
April 2, 2017
Sponsor
Mansoura University
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1. Study Identification

Unique Protocol Identification Number
NCT02423759
Brief Title
A Trial Assessing Peri-procedure Chemoprophylaxis During Transrectal Prostate Needle Biopsy
Official Title
A Randomized Controlled Trial Comparing Rectal Swab Culture Based Chemoprophylaxis Versus Combined Single-Shot Gentamycin and Ciprofloxacin Versus Ciprofloxacin Alone for Peri-procedure Chemoprophylaxis During Transrectal Prostate Biopsy.
Study Type
Interventional

2. Study Status

Record Verification Date
April 2017
Overall Recruitment Status
Completed
Study Start Date
April 2015 (undefined)
Primary Completion Date
January 16, 2017 (Actual)
Study Completion Date
April 1, 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Mansoura University

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The aim of the study is to evaluate whether changing antibiotic prophylaxis from fluoroquinolones alone to fluoroquinolones plus gentamicin 160mg single IM dose or targeted antibiotic prophylaxis according to rectal swab culture would influence infectious complication rates in those men undergoing transrectal ultrasound-guided prostate biopsy.
Detailed Description
Introduction Transrectal ultrasound (TRUS) guided prostate biopsy is the standard procedure for the histological diagnosis and grading of prostate cancer that consequently help in providing the appropriate line of treatment. Risks of infectious complications post TRUS-guided biopsy have increased in the last years. In their study, a total of 5798 TRUS-guided biopsies performed between 2002 and 2011. Increased incidence of infectious complications is noted from 0.52 infections per 100 biopsies between 2002 and 2009 to 2.15 infections per 100 biopsies between 2010 and 2011 (P< 0.001). The commonest organism found to be responsible for these infectious complications is Escherichia coli (E. Coli). The American Urological Association best practice policy statement recommends antibiotic prophylaxis prior to transrectal prostate biopsy. The current practice is to give patients a dose of an oral fluoroquinolone (FQ) 30 to 60 minutes before biopsy and to be continued for 2 to 3 days after. Recent studies show that 2% of patients will develop febrile urinary tract infection or even urosepsis and require hospitalization for intravenous antibiotics . There is considerable concern regarding the rising incidence of community-acquired antibiotic-resistant organisms. It is proposed that resistant organisms are introduced into the bladder and the blood stream from the rectum during the procedure that's why patients already colonized with these resistant organisms may be at higher risk. Thereby, some authors suggest a targeted rectal swab culture before (TRUS)-guided biopsy then giving the appropriate antibiotic prophylaxis aiming at reducing post biopsy infection rates while minimizing unnecessary broad-spectrum antibiotic use. Retrospective data showed that septicemia was seen in 24 of 300 (8%) and 15 of 897 (1.7%) in patients receiving peri-procedure ciprofloxacin alone and patients receiving ciprofloxacin plus single IV dose of amikacin injection respectively (p=0.001). E. Coli resistant to quinolones was responsible for 33 of 39 (84.6%) septicemic cases. In a retrospective study in UK, 12.9% developed infectious complications following prostate biopsy in patients receiving co-amoxiclav and gentamycin. In another retrospective study, hospitalization rate due to post-biopsy infections was 3.8% compared to 0.6% (p=0.001) in patients receiving the standard ciprofloxacin and augmented prophylaxis with ciprofloxacin plus single IM 80mg gentamycin respectively. Of the admitted patients who received standard prophylaxis, 73% had fluoroquinolone resistant E. Coli urinary infection and/or bacteremia and only 9% had strains resistant to gentamicin. Multivariate analysis showed that the standard regimen was significantly associated with hospital admission due to post-biopsy infection. The augmented regimen resulted in a cost savings of $15,700 per 100 patients compared to the standard regimen. Diabetes was found in 4% of the fluoroquinolone sensitive group vs 14.7% of the resistant group (p < 0.001). Biopsy history was not associated with resistance. Urosepsis is a systemic reaction of the body to a bacterial infection of the urogenital organs with the risk of life-threatening events including shock. Systemic inflammatory response syndrome (SIRS) criteria are defined as 2 or more of the following variables; increase in body temperature to 38°C or more, heart rate of more than 90 beats per minute, respiratory rate of more than 20 per minute or arterial carbon dioxide tension (PaCO2) less than 32mm Hg and abnormal white blood cell count (>12,000/µL or < 4,000/µL) Aim of the work; The aim of the study is to evaluate whether changing antibiotic prophylaxis from fluoroquinolones alone to fluoroquinolones plus gentamicin 160mg single IM dose or targeted antibiotic prophylaxis according to rectal swab culture would influence infectious complication rates in those men undergoing transrectal ultrasound-guided prostate biopsy.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Benign Prostate Hyperplasia
Keywords
Chemoprevention

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
510 (Actual)

8. Arms, Groups, and Interventions

Arm Title
ciprofloxacin
Arm Type
Active Comparator
Arm Description
standard chemoprophylaxis [500mg ciprofloxacin twice daily for 3 days]
Arm Title
ciprofloxacin and gentamycine
Arm Type
Experimental
Arm Description
Augmented Chemoprophylaxis [standard chemoprophylaxis plus 160mg]
Arm Title
culture based chemoprophylaxis
Arm Type
Experimental
Arm Description
Patients will receive antibiotic according to rectal swab culture at time of biopsy and then after for 3 days.
Intervention Type
Drug
Intervention Name(s)
ciprofloxacin
Other Intervention Name(s)
standard chemoprophylaxis
Intervention Description
500mg ciprofloxacin twice daily starting the day before biopsy and continued for 3 days after
Intervention Type
Drug
Intervention Name(s)
ciprofloxacin and gentamycine
Other Intervention Name(s)
standard chemoprophylaxis plus gentamicin
Intervention Description
standard chemoprophylaxis plus gentamicin 160mg intramuscular once just before the biopsy
Intervention Type
Drug
Intervention Name(s)
culture based chemoprophylaxis
Intervention Description
Patients will receive antibiotic according to rectal swab culture at time of biopsy and then after for 3 days.
Primary Outcome Measure Information:
Title
occurrence of post procedure infectious complications
Description
occurrence of post procedure infectious complications (e.g urosepsis and local genital or prostate infectious complications). Sepsis is identified as occurrence of two or more of SIRS criteria.
Time Frame
2 weeks
Secondary Outcome Measure Information:
Title
flouroquinolones resistance in rectal carriage
Description
identification of the prevalence of flouroquinolones resistance in rectal carriage in this subset of patients and post procedure non-infectious complications.
Time Frame
2 weeks
Title
post procedure non-infectious complications
Time Frame
2 weeks

10. Eligibility

Sex
Male
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Prothrombin concentration > 70% Platelet count > 100.000/cm Exclusion Criteria: Acute prostatitis (positive symptoms and signs) Patients with compromised renal function (serum creatinine >1.6 mg/dl) Uncontrolled DM Patients on immunosuppressive therapy Active steroid intake Untreated bleeding diathesis
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ahmed M Elshal, MD
Organizational Affiliation
Mansoura University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Urology and Nprhology Center
City
Mansoura
State/Province
Aldakahlia
ZIP/Postal Code
35516
Country
Egypt

12. IPD Sharing Statement

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A Trial Assessing Peri-procedure Chemoprophylaxis During Transrectal Prostate Needle Biopsy

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