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The effect of aromatherapy with orange essential oil on pain intensity, nausea, and vomiting following adenotonsillectomy

Phase 2
Recruiting
Conditions
Tonsillectomy.
Hypertrophy of tonsils
J35.1
Registration Number
IRCT20200617047805N1
Lead Sponsor
Islamic Azad University
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
96
Inclusion Criteria

Children undergoing adenotonsillectomy
Age between 6 to 12 years
No history of respiratory problems
Nausea and vomiting despite receiving antiemetic drugs and 30 minutes after receiving it

Exclusion Criteria

History of allergic rhinitis
The long time history of digestive problems
History of respiratory and skin allergies and dermatitis in children and mothers
Chronic pain in children

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
The intensity of pain. Timepoint: 30 minutes, 3, 6 and 12 hours after the intervention. Method of measurement: Based on Visual Scale (VAS).;Nausea-vomiting. Timepoint: 30 minutes, 3, 6 and 12 hours after the intervention. Method of measurement: Based on the Visual Scale (VAS) and Rhodes Nausea-vomiting Intensity Questionnaire.
Secondary Outcome Measures
NameTimeMethod
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