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Compare adequate intraoperative fluid therapy with dexamethasone on the incidence and severity of nausea and vomiting after general

Not Applicable
Conditions
Anesthesia.
Symptoms and signs involving the digestive system and abdomen
R10-119
Registration Number
IRCT2016122019359N8
Lead Sponsor
Vice Chancellor for Research, North Khorasan University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
120
Inclusion Criteria

patients should be alert; having class 1 and class 2 of America Society of Anesthesiology (ASA) score
Exclusion criteria: the patients who weigh more than 90 kg; diabetics; with underlying gastrointestinal disease; those who had used anti-nausea and anti-vomiting drugs in pre-operative 24 hours before the surgery; those who were not fasting; those with middle ear disease; those who had more than 20% of baseline drop in blood pressure after spinal anesthesia; history of nausea and vomiting during the past 24 hours

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Severity of nausea. Timepoint: During the surgery, 2 hour after the surgery, 6 hour after the surgery. Method of measurement: self-report scale.;Severity of vomiting. Timepoint: During the surgery, 2 hour after the surgery, 6 hour after the surgery. Method of measurement: self-report scale.
Secondary Outcome Measures
NameTimeMethod
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