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Comparison of the effect of aromatherapy with lavender and clove essential oil on labor pain and anxiety

Comparison of the effect of lavender and clove essential oil on the intensity of pain and anxiety of the first stage of labor

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20230301057585N1
Enrollment
159
Registered
2023-03-10
Start date
2023-04-04
Completion date
Unknown
Last updated
2023-04-03

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

Conditions

pain and anxiety of the first stage of labor.

Interventions

Intervention 1: First Intervention group: Aromatherapy with lavender essential oil with a concentration of 2% was purchased from Barich Essential Oil Company, which is impregnated with gas to the exte

Sponsors

Gonabad University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 35 Years

Inclusion criteria

Inclusion criteria: Women with first and second pregnancy, aged 18-35 years, pregnant with single fetus , having a normal delivery, 38-42 weeks of pregnancy, cephalic presentation, cervical dilatation more than 3 cm. No history of asthma, sensitivity and allergy according to mother's statements. Absence of disease and complications of pregnancy and obstetrics (such as: pre-eclampsia - chorioamnionitis - known liver, gallbladder and respiratory disease, decollement and abnormal heartbeat of the fetus at the beginning of the study), Not having smell problems and allergies to herbal medicines according to the person. Not having a known anxiety and depression disease according to the person's statements in the medical history and the mother's file. Not having migraines according to the mother's statements in the medical history. Not receiving medical painkillers 3 hours before the start of the study. There is no history of infertility and thyroid disease according to the person's statements in the medical history and the mother's file. Informed consent of women to participate in the study

Exclusion criteria

Exclusion criteria: Mother's non-cooperation in completing the checklist and expressing her pain Departure from the natural course of labor Having an emergency caesarean section Allergic to essential oil Fetal weight less than 2.5 kg or more than 4 kg

Design outcomes

Primary

MeasureTime frame
Labor Pain score. Timepoint: At the beginning of the study, dilation 4-5 cm , dilatation 8-10 cm. Method of measurement: Visual Analogue Scale (VAS).;Anxiety score. Timepoint: At the beginning of the study, dilation 4-5 cm , dilatation 8-10 cm. Method of measurement: Spielberger anxiety questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactNiloofar SadeghAhmadi

Gonabad University of Medical Sciences

Niloofarahmadi97@gmail.com+98 51 3864 9954

Outcome results

None listed

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