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Cefazolin Antibiotic Prophylaxis in Ventricular Shunt Surgery: Determination of Cerebrospinal Fluid Concentration During Valve Implantation (CC -PIV)

U

University Hospital, Strasbourg, France

Status

Not yet enrolling

Conditions

Hydrocephaly
CSF Shunts
Antibiotic Prophylaxis

Treatments

Other: Cefazolin antibiotic prophylaxis

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

The objective is to determine the concentration of cefazolin in the cerebrospinal fluid after a recommended antiobiotic prophylaxis by 2g of cefazolin. Our main hypothesis is that the concentration is insufficient to protect the valve from infections.

The secondary objective is to compare our results to known pharmacokinetic models of cefazolin diffusion in the literature. If differences are found we would like to search clinical features that could explain it.

Enrollment

15 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Age >18 years and programmed for a ventricular shunt surgery at the Hautepierre university hospital in Strasbourg.

Exclusion criteria

  • Age <18 years old
  • Pregnant women
  • Infected patients
  • Known cefazolin allergy
  • Other molecule used for the antibiotic prophylaxis
  • Guardianship or conservatorship
  • Patients under curative antibiotherapy
  • Non sterile pre operative CSF
  • Refusal to participate

Trial design

Primary purpose

Health Services Research

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

15 participants in 1 patient group

Cefazolin antibiotic prophylaxis in ventricular shunt surgery
Experimental group
Treatment:
Other: Cefazolin antibiotic prophylaxis

Trial contacts and locations

1

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Central trial contact

Baptiste BOUCHIER, MD

Data sourced from clinicaltrials.gov

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