pain. Pain, unspecified
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 18 yr of age or older Lack of allergy to plants and the aroma No use of palliative about 6 hours ago No damaged skin at the desired part lake of known allergies or sensitivities to lidocaine, prilocaine or other local anesthetic Lack of olfactory disorder Lack of addiction to drugs and alcohol Having a minimum reading and writing literacy Being conscious patient Lack of severe pain in other places
Exclusion criteria
Exclusion criteria: Dissatisfaction to continue the research Death or hospitalization in other wards Allergy or critical reaction during the study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pain. Timepoint: Measuring the severity of pain caused by needle insertion before any intervention and after intervention with topical lidocaine gel and intervention with the aromatherapy with Salvia officinalis. Method of measurement: Visual Analog Scale. | — |
Countries
Iran (Islamic Republic of)
Contacts
Gonabad University of Medical Sciences