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Lemon essential oil on patients admitted to the intensive care unit

Effectiveness of Aromatherapy with lemon essential oil on delirium, pain and appetite in patients admitted to the intensive care unit

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20250125064510N1
Enrollment
60
Registered
2025-04-13
Start date
2025-05-22
Completion date
Unknown
Last updated
2025-07-21

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

Conditions

Patients admitted to the intensive care unit. Encounter for other specified special examinations

Interventions

Intervention 1: Intervention group: Inhaling lemon essential oil (Barij Essential Oil Company) using aromatherapy pads that can be used in hospital environments next to the patients pillow for thirty

Sponsors

Iran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Over 18 years old Hospitalization for at least 7 days in the intensive care unit Probability of delirium according to clinical assessment Consent of the patient or the patient's legal guardian to participate in the study by completing an informed consent form. Hemodynamic stability of the patient Patients who are receiving oral nutrition and are conscious.

Exclusion criteria

Exclusion criteria: Allergic reaction to lemon essential oil Patient's lack of cooperation or unwillingness to participate in the study at any stage of the study Hospitalization for less than 7 days or death during the study Unconscious patients

Design outcomes

Primary

MeasureTime frame
Pain intensity using the visual pain scale. Timepoint: Beginning of the study and the fifth day of the study. Method of measurement: Visual pain scale.;C-reactive protein. Timepoint: Beginning of the study and the fifth day of the study. Method of measurement: The enzyme-linked immunosorbent assay (ELISA).

Secondary

MeasureTime frame
Delirium. Timepoint: Beginning of the study and the fifth day of the study. Method of measurement: Confusion Assessment method for the ICU.;Appetite. Timepoint: Beginning of the study and the fifth day of the study. Method of measurement: Appetite Visual Analog Scale.;Erythrocyte Sedimentation Rate. Timepoint: Beginning of the study and the fifth day of the study. Method of measurement: Westergren.;Serum albumin. Timepoint: Beginning of the study and the fifth day of the study. Method of measurement: Bromocresol green colorimetric method.;Body Mass Index. Timepoint: Beginning of the study and the fifth day of the study. Method of measurement: Weight in kilograms divided by height in meters squared.;Arm circumference size. Timepoint: Beginning of the study and the fifth day of the study. Method of measurement: Arm circumference in the midpoint between the shoulder and elbow using a tape measure.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSeyed Mohammad Aghaeinejad

Iran University of Medical Sciences

m.aqaei@yahoo.com0098 21 64351

Outcome results

None listed

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