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Trial of Randomized Antibiotic Administration in Percutaneous Nephrolithotomy

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Northwell Health

Status and phase

Completed
Phase 3

Conditions

Kidney Stones

Treatments

Drug: Clindamycin
Drug: Ampicillin/Gentamicin
Drug: Fluoroquinolones
Drug: cephalosporins

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

The Investigators objective is to compare the clinical efficacy of a single-day protocol with a short-course protocol for PCNL. The investigator hope is to reduce the use of possibly unnecessary prolonged antibiotic use, reduce hospital costs and prevent the further propagation of resistant microbes.

Full description

For large renal stone burdens and/or complex stones, Percutaneous Nephrolithotomy (PCNL) has become the mainstay for treatment, replacing open kidney stone surgery since it's introduction in 1976. However, PCNL is not without its complications, specifically infectious. The procedure carries up to 25% incidence of infectious complications with approximately 1% rate of severe sepsis even with completely sterile conditions. Therefore, the use of antibiotics becomes paramount, but to date there are no PNCL specific guidelines for the appropriate duration and class of antibiotics. This fact leaves the practicing urologists to their own subjective experiences to the guide them. In addition, in an age where there are increasing numbers of resistant microbes the judicious use of antibiotics is in even more paramount.

The investigators of this project, purpose a randomized intention to treat prospective study to explore the duration and type of antibiotics in a larger population then previously studied. The investigators hypothesize that there will be no difference in complications between two groups: 1) 24 hours of perioperative antibiotics versus 2) Continued antibiotics until the removal of any external catheters. The investigators will model the antibiotics choices and duration after the 2013 American Urological Association, (AUA) Urologic Surgery Antimicrobial Prophylaxis recommendations, modified by our local antibiogram as necessary. The investigators' objective is to compare the clinical efficacy of a single-day protocol with a short-course protocol for PCNL. Our hope is to reduce the use of possibly unnecessary prolonged antibiotic use, reduce hospital costs and prevent the further propagation of resistant microbes.

Antibiotic detail: cephalosporins or aminoglycoside + metronidazole or clindamycin and the alternative for allergies being aminoglycoside/ sulbactam or fluoroquinolone

Looking at the same drugs and doses the variable is the timeframe of the medication

Enrollment

98 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Patients >18 years old
  • Negative urine culture within 1 month prior to procedure
  • Renal Calculi which would optimally require PCNL for treatment.

Exclusion criteria

  • Patients <18 years old.
  • Patients who are not able to give consent for study
  • Patients currently on antibiotics immediately prior to the procedure
  • Previous history of sepsis or SIRS from stone manipulations
  • Foley catheter in place for greater than 1 week duration
  • Patients under going planned, multi-staged procedures
  • Immunosuppressed patients

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

98 participants in 2 patient groups

Antibiotics for a 24 hour period
Active Comparator group
Description:
Antibiotics for a 24 hour period Intervention drug to be determined based on patient history etc.
Treatment:
Drug: cephalosporins
Drug: Fluoroquinolones
Drug: Ampicillin/Gentamicin
Drug: Clindamycin
Continued antibiotics
Active Comparator group
Description:
Continued antibiotics until the removal of any external catheters Intervention drug to be determined based on patient history etc.
Treatment:
Drug: cephalosporins
Drug: Fluoroquinolones
Drug: Ampicillin/Gentamicin
Drug: Clindamycin

Trial documents
1

Trial contacts and locations

2

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Data sourced from clinicaltrials.gov

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