Clinical trial to compare two methods of giving intravenous fluid therapy during the operation in open abdominal surgeries
Not Applicable
Completed
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2021/04/033021
- Lead Sponsor
- Department of Anesthesiology and Intensive Care Maulana Azad Medical College
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Patients falling under the American Society of Anesthesiologists(ASA) physical status classes I, II, and III undergoing elective and emergency exploratory laparotomy under general anesthesia
Exclusion Criteria
1. Pregnant patients
2. Preexisting ischemic or valvular heart disease, heart failure, or cardiac arrhythmias
3. Chronic kidney disease
4. Preexisting coagulopathies
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Postoperative plasma lactate levelTimepoint: Postoperative plasma lactate level- 1 hour after the end of surgery
- Secondary Outcome Measures
Name Time Method