A clinical trial to study fluid therapy in very sick patients with metabolic alterations comparing ringer lactate and acetate solutio
Phase 4
Recruiting
- Conditions
- Health Condition 1: null- Critically ill patients having metabolic acidosis
- Registration Number
- CTRI/2017/08/009261
- Lead Sponsor
- eeru Sahni
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
All adult patients admitted to Main ICU with metabolic acidosis i.e. pH less than 7.29 and standard HCO3- less than19mmol/l).
Exclusion Criteria
Patients with contraindication to large volume fluid resuscitation for example: anuria secondary to renal failure, left ventricular failure.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Primary outcome of the study is the time to correction of pH till 7.30 in critically ill patients with metabolic acidosis.Timepoint: 2 hours
- Secondary Outcome Measures
Name Time Method Secondary outcome of the study will be to assess change in pH, lactate level, bicarbonate and base deficit during the period of resuscitation (that is, the time to correction of pH till 7.30), volume of IV fluid used for correction and also the total cost of IV fluid used for resuscitation.Timepoint: 2 hours