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Comparative effect of Ondansetron and acupressure on nausea and vomiting

Not Applicable
Completed
Conditions
ausea and vomiting.
Nausea and vomiting
Registration Number
IRCT201603155596N3
Lead Sponsor
orestan University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
120
Inclusion Criteria

elective cesarean; being NPO 8 to 12 hours before surgery; being NPO 6 hours after surgery; lack of symptomatic digestive disease; lack of motion sickness; lack of dizziness; lack of cardiovascular disease; lack of pulmonary disease; lack of middle ear disease; lack of diabetes; lack of infectious disease; lack of fever; lack of hypertension; lack of lateral surgery except for cesarean; lack of carpal tunnel syndrome; not taking alcohol; not taking immunosuppressive drugs; lack of long or unusual bleeding; lack of hemoglobin level less than 10 mg/dl; not receiving drugs except for antibiotics and analgesics in form of Diclofenac suppository daily 6 hours after surgery; American Society of Anesthesiologists classes I and II patients; patients with mild diseases without any performance limitation; patients with controlled disease; controlled diabetes or hypertension without systemic effects; smoking without chronic obstructive pulmonary disease; mild obesity; pregnant women aged 18 to 45 years with 38 to 40 weeks pregnant; exclusion criteria: lack of desire to continue cooperation in each step of research; change in surgery trend such as needing to general anesthesia; outbreak of any problem and uncommon and unexpected complication; severe nausea and vomiting according to anesthesiologist’s diagnosis; emergency cesarean; having lateral surgery except for cesarean; the weight more than 100 kg and less than 50 kg.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
ausea. Timepoint: During the surgery, recovery, and in female surgical ward till 6 hours after the surgery. Method of measurement: Using checklist, asking questions and visual scale criteria.
Secondary Outcome Measures
NameTimeMethod
Outbreak of vomiting. Timepoint: During the surgery, recovery, and in female surgical ward till 6 hours after the surgery. Method of measurement: Using checklist, asking questions and visual scale criteria.;Number of episodes of vomiting. Timepoint: During the surgery, recovery, and in female surgical ward till 6 hours after the surgery. Method of measurement: Using checklist, asking questions and visual scale criteria.
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