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Comparison of two types of intravenous fluid for resuscitation during surgery

Phase 4
Conditions
Health Condition 1: null- ASA I-II patients with two or more long bone fracture
Registration Number
CTRI/2017/11/010417
Lead Sponsor
Department of Anesthesia Post Graduate Institute of Medical Education Research
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Open to Recruitment
Sex
Not specified
Target Recruitment
50
Inclusion Criteria

fracture femur scheduled for interlocking or percutaneous nailing under anesthesia

Exclusion Criteria

Associated abdominal injury,

severe head injury,

renal failure

Electrolyte imbalance

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
The primary outcome would be the change in base excess from 0 to 24 hours & Upon arrival to operation theatre â??time 0 hoursâ??.Timepoint: intra operatively, in recovery, 12 hrs and 24 hrs
Secondary Outcome Measures
NameTimeMethod
serum osmolality, serum electrolytes, lactate, base excess, pH, urea and creatinine levelsTimepoint: at 24 hrs
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