Actively Recruiting

Phase 1
Age: 18Years +
All Genders
NCT05001750

Prophylactic Antibiotics Useful With Antibiotic Impregnated External Ventricular Drains (EVDs)?

Led by Montefiore Medical Center · Updated on 2026-02-02

84

Participants Needed

1

Research Sites

259 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The principal objective of this study is to compare the incidence of ventriculostomy related infections (VRIs) in patients who receive twenty-four hours of antibiotics, beginning no more than sixty minutes prior to EVD placement, to the incidence of VRIs in patients who also receive a pre-procedural dose of antibiotics with continued dosing of antibiotics for the duration of the external ventricular drain (EVD). At this time, the duration of prophylactic antibiotic use with antibiotic impregnated EVDs is unknown.

CONDITIONS

Official Title

Prophylactic Antibiotics Useful With Antibiotic Impregnated External Ventricular Drains (EVDs)?

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients over the age of 18 years
  • Patients diagnosed with subarachnoid hemorrhage, intracerebral hemorrhage, or acute ischemic stroke who need an external ventricular drain (EVD) for treatment
  • Patients who may require EVD replacement due to failure and will be re-dosed with antibiotics before catheter exchange
Not Eligible

You will not qualify if you...

  • Patients who were on antibiotics within the week prior to admission
  • Patients with leukopenia (white blood cell count less than 5000) at the start of the study
  • Patients who show signs of meningitis, ventriculitis, or other infections at the time of presentation
  • Patients who are pregnant or prisoners
  • Patients under 18 years of age

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Montefiore Medical Center

The Bronx, New York, United States, 10452

Actively Recruiting

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Research Team

D

David C Altschul, MD

CONTACT

G

Genesis Liriano

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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