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Extracts of lavender on pain and anxiety in patients with burns

The effect of inhalation aromatherapy with lavender extract on pain and anxiety in burn patients: a randomized clinical trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2017030632129N3
Enrollment
120
Registered
2017-05-17
Start date
2017-04-21
Completion date
Unknown
Last updated
2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Burn. Burns and corrosions of external body surface

Interventions

Intervention 1: The scent of lavender is used in the intervention group. Intervention 2: The scent of lavender is used in the intervention group.
Treatment - Other
The scent of lavender is used in the intervention group

Sponsors

Vice Chancellor for Research and Technology of Hamadan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 55 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: degree burns 2, alertness naturally able to speak clearly, confirmed the doctor's lack of a ban on entry to the study, lack of sensitivity to herbal medicines, non-drug addiction (based on patient testimony), lack of brain tumor, stroke head, epilepsy, lack of mental disorders, there is no problem of smell, lack of focus pain of others, the use of perfume by the patient simultaneously, burns 30% of body surface area based on the criteria Lund and Browder, 48 hours of patient past the hospital, the fire does not burn because, aged 18 to 55 years. Exclusion criteria: Use of herbal medicines by the patients, creating any disturbance of smell, causing respiratory problems and allergic withdraw from the study at any stage of the study, participated in a similar study at the same time (aromatherapy), based on the scale, visual analogue pain less than 3, less patient anxiety score of 20 on a scale of Der Burger.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Pain. Timepoint: 3 times in 3 days. Method of measurement: pain Chart.;Anxiety. Timepoint: 3 times in 3 days. Method of measurement: Spielberger questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAzim Azizi

Hamadan University of Medical Sciences

a.azizi@umsha.ac.ir+98 81 3838 0150

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026