comparison of newer and higher dose antibiotics combination therapy with old and standard antibiotics combination therapy in critically ill patients who are carbapenem resistant enterobacteriaceae (CRE)
- Conditions
- Health Condition 1: R799- Abnormal finding of blood chemistry, unspecified
- Registration Number
- CTRI/2022/09/045736
- Lead Sponsor
- Department of Anaesthesiology and Critical and Care Jawaharlal Nehru Medical College AMU Aligarh
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
1.Patient having sepsis and SOFA score of 2 or more than 2 at the time of admission in icu/ccw.
2.There should be an isolates of carbapenem resistant enterobacteriaceae (CRE) positive either from Blood, tracheal aspirates, urine or abdominal pus culture.
3.Patient on any empirical antibiotics except current combination therapy .
1.Patient who is not having sepsis and having SOFA score of less than 2. Non Carbapenem resistant enterobacteriaceae (CRE) patients.
3.Patient who expire within 48 hours of starting the combination
therapy.
4.Patient having sensitivity to the drug use .
5.Covid -19 positive patients
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To see the changes in sequential organ failure assessment (SOFA) score at zero hour and after 48 hours of starting combination therapies meropenem plus colistin and high dose tigecycline plus colistin in carbapenem resistant enterobacteriaceae positive cases.Timepoint: 2 days
- Secondary Outcome Measures
Name Time Method To see the microbiological eradication of carbapenem resistant enterobacteriaceae on 5th day and to report any mortality within 5 days of starting the antibiotics combination therapies .Timepoint: 5 days
Related Research Topics
Explore scientific publications, clinical data analysis, treatment approaches, and expert-compiled information related to the mechanisms and outcomes of this trial. Click any topic for comprehensive research insights.