Investigating and comparing the severity and prevalence of ventilator-induced pneumonia in patients taking famotidine and pantoprazole in the intensive care unit

Phase 3

Recruiting

• Conditions: ventilator-induced pneumonia.; ventilator-associated pneumonia; J95.851

• Registration Number: IRCT20231220060484N2
• Lead Sponsor: Islamic Azad University

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 27 May 2024

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 124

Inclusion Criteria

The inclusion criteria for the study of patients include the use of patients aged 18 to 80 years in intensive care units who have mechanical ventilation for at least 48 hours.

Exclusion Criteria

Patients with active pulmonary infection, patients with immunosuppression, patients with liver problems, renal problems (high creatinine levels), people with a history of sensitivity, and those with active gastrointestinal bleeding will not be included.

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Pneumonia incidence is measured by the occurrence of infection or its non-occurrence. Timepoint: Investigating the occurrence of pneumonia after 48 hours of hospitalization. Method of measurement: Qualitative measurement with CT scan or Chest X-ray criteria / Quantitative measurement with CPIS criteria.