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The effect of oral lavender essential oil on menopausal symptoms, serum lipid profile, and cortisol concentration in postmenopausal women

The effect of oral lavender essential oil on menopausal symptoms, serum lipid profile, and cortisol concentration in postmenopausal women: A triple-blind, randomized, controlled trial

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20131009014957N13
Enrollment
72
Registered
2022-04-27
Start date
2022-05-10
Completion date
Unknown
Last updated
2022-05-02

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

Conditions

Menopausal symptoms. Menopausal and other perimenopausal disorders

Interventions

Intervention 1: Intervention group: Recipient of gelatin capsules containing 80 mg of lavender essential oil. The course of drug consumption is 60 days and one capsule is consumed daily after a meal,

Sponsors

Tabriz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
45 Years to 60 Years

Inclusion criteria

Inclusion criteria: Willingness to participate in the study Be literate enough to fill out a questionnaire or presence of a literate person in the family Having a normal menopause Women who were menopause less than 6 years ago Having a minimum of 45 and a maximum of 60 years of age Earning a minimum score of 15 and a maximum of 42 in the Green assessment

Exclusion criteria

Exclusion criteria: Use of tobacco and alcoholic beverages and herbal medicines Existence of stressors such as the death of first-degree relatives in the last 6 months and job loss Existence of malignant disease Recent history of surgery and trauma Lavender consumption during the 3 months before the study Use of hormone therapy during the past 6 months Having known physical and mental illnesses according to self-expression (depression, uncontrolled diabetes, cardiovascular diseases)

Design outcomes

Primary

MeasureTime frame
Green scale symptoms score in postmenopausal women. Timepoint: Before and after intervention. Method of measurement: Green questionnaire.;Serum cortisol levels. Timepoint: Before and after intervention. Method of measurement: Enzyme-linked immunosorbent assay (ELISA) method by ELISA kits.

Secondary

MeasureTime frame
Reported possible side effects. Timepoint: After the intervention. Method of measurement: Checklist of possible side effects.;The level of satisfaction with the intervention received. Timepoint: After the intervention. Method of measurement: Satisfaction checklist received from the intervention.;Serum levels of lipid profile. Timepoint: Before and after intervention. Method of measurement: By spectrophotometric method with device with Alcyon 300 model and Pars test kit.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Azizeh Farshbaf-Khalili

Tabriz University of Medical Sciences

farshbafa@tbzmed.ac.ir+98 41 3336 1928

Outcome results

None listed

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