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Investigating the effect of aromatherapy in abdominal surgery

Not Applicable
Recruiting
Conditions
Multiple sclerosis.
Demyelinating diseases of the central nervous system
Registration Number
IRCT20180103038211N9
Lead Sponsor
Arak University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
60
Inclusion Criteria

Abdominal Surgery
Have a healthy sense of smell

Exclusion Criteria

History of smoking
History of allergy and allergy to medicinal herbs
A history of asthma or respiratory illness
The history of a new crisis, such as the death of a first-degree relative, the divorce of a person or parent during the past six months
History of previous surgery

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
evel of anxiety. Timepoint: Measure one hour before surgery, 20 minutes before surgery, one hour and two hours after full vigilance after surgery. Method of measurement: Anxiety Visual Analog Scale.;Nausea. Timepoint: one hour and two hours after full vigilance after surgery. Method of measurement: Visual Analog Scale Nausea.;Vomiting. Timepoint: one hour and two hours after full vigilance after surgery. Method of measurement: Measures based on occurrence or non-occurrence.
Secondary Outcome Measures
NameTimeMethod
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