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Investigation of the Effect of Local Amitriptyline on the Severity of Gag Reflex

Phase 2
Recruiting
Conditions
Gag Reflex.
Symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified
R00-R99
Registration Number
IRCT20190608043843N1
Lead Sponsor
Islamic Azad University
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
48
Inclusion Criteria

People whose Nausea rate is Higher than 2 using the GTPI Standard
Eat Breakfast Two Hours before the Test

Exclusion Criteria

Existence of Systemic Diseases
Drug Allergy(Amitriptyline or lidocaine)
Pregnant and Lactating Women

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Reduction of Gag reflex. Timepoint: In the amitriptyline group before the intervention and 30 minutes after the intervention in the lidocaine group before the intervention and 5 minutes after the intervention, the nausea reflex is examined. Method of measurement: Gag Trigger Point Index (GTPI).
Secondary Outcome Measures
NameTimeMethod
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