MedPath

Evalution of the granisetron instead of ondansetron in the emergency room

Phase 1
Conditions
ausea and vomiting.
Nausea and vomiting
Registration Number
IRCT20230726058930N3
Lead Sponsor
Ahvaz University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
All
Target Recruitment
100
Inclusion Criteria

Nausea
Vomit

Exclusion Criteria

Patients with symptoms such as headaches, lateralized symptoms, and unstable vital signs.
Patients who have chest pain or ECG changes.
Patients with symptoms of Rise ICP.
Patients who have used drugs that increase serotonin (such as fluoxetine, doxepin, isomerbuxazid, amitriptyline, etc.) in the last few days.
Patients who have used drugs that increase serotonin (such as fluoxetine, doxepin, isomerbuxazid, amitriptyline, etc.) in the last few days.
Patients who have consumed grapefruit in the past 24 hours Patient does not consent to attend or continue treatment.

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
ausea and vomiting. Timepoint: 30, 15, 45, 60, 75 and 95 minutes after intravenous granisetron injection. Method of measurement: Visual Analogue Scale.
Secondary Outcome Measures
NameTimeMethod
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