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The impact of the aromatherapy with damask rose on stress, anxiety and hemodynamic parameters of patients undergoing angiography

Impact of inhalation aromatherapy with damask rose on stress, anxiety and hemodynamic parameters of patients undergoing coronary angiography One-blind randomized clinical trial in two groups (intervention and placebo)

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201702019759N8
Enrollment
98
Registered
2017-07-31
Start date
2017-08-22
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: Stress. Condition 2: Atherosclerotic heart disease. Condition 3: Anexity. Condition 4: Coronary angiography. Acute stress reaction I25.1 Generalized anxiety disorder Medical devices associated with adverse incidents in diagnostic and therapeutic use

Interventions

Intervention 1: In the intervention group, patients inhale five drops of 40% Rosa Damascus Essence on absorbent Cloth attached to their collar for 20 minutes. Intervention 2: In the placebo group, p
Treatment - Drugs
Placebo
In the intervention group, patients inhale five drops of 40% Rosa Damascus Essence on absorbent Cloth attached to their collar for 20 minutes.
In the placebo group, patients inhale five drops of distilled water are placed on an absorbent cloth attached to their collar for 20 minutes.

Sponsors

Vice chancellor of research and technology
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 64 Years

Inclusion criteria

Inclusion criteria: Candidate patients for coronary angiography in the angiographic section will be included in the following criteria: (a) first time angiography; (b) lack of critical clinical conditions; (c) non-compliance with angioplasty; (d) lack of alcohol and narcotic addiction; (E) Full person alertness and ability to answer the questioner's questions; (i) Absence of diagnosed anxiety disorder based on the physician's opinion. Patients with the following criteria will be excluded from the study: (a) aromatherapy intolerance for any cause; (b) any disorder or instability in the state of consciousness or hemodynamic Leads to the impossibility of continuing the study; (c) the reluctance to continue to participate in Study

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Hemodynamic parameter. Timepoint: Before and after the intervention. Method of measurement: Using a heart monitor and a clock.;Stress. Timepoint: Before and after the intervention. Method of measurement: Using the stress section of the dass questionnaire 21.;Anxiety. Timepoint: Before and after the intervention. Method of measurement: Using the anxiety section of DASS 21 questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Ali Bikmoradi

School of public health, Hamadan University of Medical Sciences

bikmoradi@umsha.ac.ir+98 81 1838 0439

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 15, 2026