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To assess the effectiveness of different antibiotics in lung and blood infections caused by carbapenem resistant bacteria

Not Applicable
Conditions
Health Condition 1: A415- Sepsis due to other Gram-negativeorganisms
Registration Number
CTRI/2024/02/062846
Lead Sponsor
Dr Deepak Govil
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Open to Recruitment
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

Adult more than 18 years of age with confirmed culture based diagnosis of hospital acquired pneumonia (HAP) (pneumonia developing at least 48 hours after hospital admission) and / or blood stream infection caused by CRE (Klebsiella pneumoniae, Escherichia coli) CRAB & CRPA

Received antibiotic mono and or combination therapy for at-least 48 hours as per clinician’s discretion

Exclusion Criteria

Culture positive from any site other than blood stream/ pneumonia.

Any organism other than CRE (Klebsiella pneumoniae, Escherichia coli), CRAB & CRPA isolated within 14 days of initiation/ EOT of antibiotic therapy

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
1. Clinical outcomes of patient with BSI <br/ ><br>2.Clinical outcomes of patient with HAP <br/ ><br>3.Clinical outcomes of patient with HAP plus BSI <br/ ><br>4.Microbiological outcome in patients with BSI <br/ ><br>5.Microbiological outcome in patients with HAP <br/ ><br>6.Microbiological outcome in patients with HAP plus BSITimepoint: Day 7 and day 14 or EOT from the initiation of antibiotic mono-/ combination therapy <br/ ><br>
Secondary Outcome Measures
NameTimeMethod
1.Duration of invasive mechanical ventilation (hours) <br/ ><br>2.Duration of vasopressor requirement (hours) <br/ ><br>3.Need for RRT (Yes/No) <br/ ><br>4.Length of hospital stay <br/ ><br>5.Length of ICU stay <br/ ><br>6.ICU outcome <br/ ><br>7.Hospital outcome <br/ ><br>Timepoint: 7 days and 14 days or end of treatment
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