MedPath

It is a study to compare two intravenous fluids in patients of head injury undergoing surgery using normal saline and isotonic balanced crystalloid

Phase 2
Conditions
Health Condition 1: S062- Diffuse traumatic brain injuryHealth Condition 2: S066- Traumatic subarachnoid hemorrhageHealth Condition 3: S065- Traumatic subdural hemorrhage
Registration Number
CTRI/2020/09/027624
Lead Sponsor
Department of Anaesthesiology and Critical Care
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

patients of either sex scheduled to undergo emergency craniotomy for traumatic brain injury will be enrolled

Exclusion Criteria

associated injuries (long bone fracture, thoracic or abdominal injuries), renal or coagulation dysfunctions, electrolyte imbalance, hemodynamic instability, pregnancy and lactation, difficult airway, comorbidities will be excluded from the study

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Effects on renal functions{blood urea, serum creatinine, serum electrolytes and neutrophil gelatinase-associated lipocalin(NGAL)} <br/ ><br>acid base equilibrium(pH, base excess and bicarbonate)Timepoint: baseline, induction of anaesthesia, surgical incision, bone flap removal, 1 hour after starting of surgery, closure of skin, shifting to PACU, 12 hours and 24 hours after shifting
Secondary Outcome Measures
NameTimeMethod
serum osmolarity <br/ ><br>coagulation profile(Prothrombin time, Partial thromboplastin time, International normalised ratio)Timepoint: baseline, induction of anaesthesia, surgical incision, bone flap removal, 1 hour after starting of surgery, closure of skin, shifting to PACU, 12 hours and 24 hours after shifting
© Copyright 2025. All Rights Reserved by MedPath