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The effect of inhalation aromatherapy with Damask Rose on the pain and vital signs in the patients with burn

The effect of inhalation aromatherapy with Damask Rose ( Rose Damascena) essential oil versus placebo on the pain and vital signs in the burn patients after dressing: a single blinded randomized clinical trial

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
IRCT
Registry ID
IRCT201302249759N4
Enrollment
50
Registered
2013-07-29
Start date
2013-07-06
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

Condition 1: Burns. Condition 2: Pain in Soft tissue, unspecified. Burns involving 20-29% of body surface, Burns involving 30-39% of body surface, Burns involving 40-49% of body surface Soft tissue disorder, unspecified

Interventions

Intervention 1: . Intervention1: in the first day, the base line of the vital signs and the pain of patients will be controlled in half an hour before entering into the dressing room and the patients
Treatment - Drugs
Placebo
. Intervention1: in the first day, the base line of the vital signs and the pain of patients will be controlled in half an hour before entering into the dressing room and the patients inhale 5 drops o
Intervention2: in the first day, the base line of the vital signs and the pain of patients will be controlled in half an hour before entering into the dressing room and the patients inhale 5 drops of

Sponsors

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

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: a) age18 to 65 years? b) burns degree of 2 or 2 and 3 with 15 to 45 percent burn level; c) stability of hemodynamic status; d) lack of electrical or inhalation burns; e) lack of allergy or respiratory diseases; f) lack of narcotic addiction or drug abuse. Exclusion criteria: a) Lack of patient cooperation during the intervention for any reason; b) creation dangerous conditions of disease during the intervention; c) allergy to inhalation of Damask Rose essential oil during the intervention.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Pain. Timepoint: 30 min before and 15 and 30 minutes after leaving the dressing room dressing room. Method of measurement: Visual Analog Scale.

Secondary

MeasureTime frame
Vital signs (heart rate, blood pressure and respiratory rate). Timepoint: 30 min before and 15 and 30 minutes after leaving the dressing room dressing room. Method of measurement: manual measurement and digital blood pressure device.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Ali Bikmoradi

Department of Medical Surgical Nursing

bikmoradi@umsha.ac.ir abeikmoradi@yahoo.com+98 81 1838 0439

Outcome results

None listed

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