EVALUATION OF PULSE OXYMETER PARAMETER TO PREDICT REQUIREMENT OF DRUGS TO INCREASE BLOOD PRESSURE IN PATIENTS WITH SEPSIS
Not Applicable
- Conditions
- Health Condition 1: A419- Sepsis, unspecified organism
- Registration Number
- CTRI/2023/02/049572
- Lead Sponsor
- Indraprastha Apollo Hospitals
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Age > 18 years
Clinically suspected sepsis
Adequate Fluid Resuscitation (30ml/kg)
Exclusion Criteria
Age < 18 years
Pregnant Females
inadequate fluid resuscitation ( <30ml/kg)
Already receiving vasopressor therapy
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Compare perfusion index to arterial lactate levels at T0 and T6 hours as predictor of vasopressor requirement in first 24 hourTimepoint: Compare perfusion index to arterial lactate levels at T0 and T6 hours as predictor of vasopressor requirement in first 24 hour
- Secondary Outcome Measures
Name Time Method final outcome of patients with sepsis (Discharged / Death)Timepoint: 0-28 days