Skip to content

The effect of inhalation aromatherapy with rose essential oil on anxiety level in patient undergoing coronary surgery

The effect of inhalation aromatherapy with rose essential oil on anxiety level in patient undergoing coronary surgery

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2017091919677N5
Enrollment
66
Registered
2017-11-13
Start date
2017-10-23
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

Anxiety. Behavioural syndromes associated with physiological disturbances and physical

Interventions

Intervention 1: intervention group: 3 drop of essential oils of 4% rose manufacturing of Pharmaceutical Company Barij essence with manufacturing number 714043, will be shed by the dropper on the non
Treatment - Drugs
Control group: The routine cares will be done in this patients.
intervention group: 3 drop of essential oils of 4% rose manufacturing of Pharmaceutical Company Barij essence with manufacturing number 714043, will be shed by the dropper on the non absorbent cotto

Sponsors

Vice Chancellor for Research Mazandaran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Inclusion criteria: The desire to participate in the study? Insensitivity to essential oils and aromas? have age Equal or above 18 years old? be candidate for coronary artery bypass graft surgery. Inclusion criteria: showing allergy to rose essential inhalation during the study? Occurrence of respiratory problems during intervention? unwillingness to participate in or continue the study.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Anxiety. Timepoint: Immediately before intervention,The night before the operation,one hour before operation. Method of measurement: spielberger Anxiety questionnaire.

Secondary

MeasureTime frame
Respiratory sensation and shorthness of breath. Timepoint: The night before the operation,One hour before operation. Method of measurement: Self-report questionnaire on possible complications.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactFatemeh Fazlollahpoor

Mazandaran University of Medical Sciences - Faculty of Nursing and Midwifery Nasseibeh

f.fazlollahpoor@gmail.com+98 11 4220 1376

Outcome results

None listed

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