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Colistin Versus Colistin Combined With Cefoperazone-sulbactam for Multiresistant Acinetobactor Baumannii Ventilator-associated Pneumonia Treatment

Colistin Versus Colistin Combined With Cefoperazone-sulbactam for Multiresistant Acinetobactor Baumannii Ventilator-associated Pneumonia Treatment

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07671755
Acronym
CRAB
Enrollment
80
Registered
2026-06-26
Start date
2025-02-01
Completion date
2026-04-30
Last updated
2026-06-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Clinical Response, Radiological Response

Keywords

multidrug-resistant Acinetobacter baumannii, ventilator-associated pneumonia, intensive care unit

Brief summary

This study aims to evaluate clinical outcomes of colistin versus colistin in combination with cefoperazone-sulbactam for patients with MDR-AB VAP treatment.

Detailed description

MDR-AB (multidrug-resistant Acinetobacter baumannii) has been an increasingly common cause of ventilator-associated pneumonia (VAP) in intensive care unit (ICU). Colistin remains the last available antibiotic choice. Unfortunately, colistin monotherapy is often inadequate for microbiologic eradication and a risk factor of nephrotoxicity and for heteroresistance.

Interventions

DRUGcolistin plus cefoperazone-sulbactam combination group

Combination therapy

DRUGColistin

Monotherapy

Sponsors

Shaheed Mohtarma Benazir Bhutto Institue of Trauma
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* Patients with a diagnosis of VAP due to A. baumannii

Exclusion criteria

* patients who had polymicrobial VAP * Patients with pre-existing severe renal failure and/or abnormal liver function tests * Patients allergic to colistin or cefoperazone-sulbactam

Design outcomes

Primary

MeasureTime frameDescription
Clinical responsewithin one weekClinical response was defined as observable improvement in the patient's clinical signs/symptoms, including absence of fever (temp\<38ºC) for three consecutive days or more, and decreasing amount and purulence of tracheal secretions

Secondary

MeasureTime frameDescription
Radiological responsewithin one weekRadiological response was defined as improvement/resolution of pulmonary infiltrates, as noted on chest x-rays following treatment.

Countries

Pakistan

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 27, 2026