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

Not Applicable

• Conditions: Anesthesia.; R10-119; Symptoms and signs involving the digestive system and abdomen

• Registration Number: IRCT2016080219359N6
• Lead Sponsor: Vice Chancellor for Research, North Khorasan University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 22 February 2018

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

Name	Time	Method
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.