Comparison of two methods to decide amount of intravenous fluids to be given in open abdominal surgeries.
Not Applicable
- Conditions
- Health Condition 1: C569- Malignant neoplasm of unspecifiedovary
- Registration Number
- CTRI/2018/12/016543
- Lead Sponsor
- Max Superspecilaity Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Patients planned for elective non-gastrointestinal open surgeries
Exclusion Criteria
1.Patient refusal.
2.Surgeries with an expected intraoperative lood loss of more than 30% of blood volume.
3.Surgeries likely to exceed 8 hours duration.
4.Any patient with a preoperative NYHA status of more than II or a high cardiac risk stratification.
5.Baseline hemoglobin of less than 10 gm/dl.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Duration of stay in the intensive care unit postoperativelyTimepoint: Post induction, intraoperative parameters and 2 hours after surgery
- Secondary Outcome Measures
Name Time Method Secondary outcome will be time of first passage of flatus and incidence of postoperative complications.Timepoint: From end of surgery till discharge from hospital