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Study of Effect of Citrus aurantium Aroma on Severity of Labor Pain and Anxiety

Study of Effect of Citrus aurantium Aroma on Severity of Labor Pain and Anxiety in Patients Admitted to Vali-e Asr Hospital, Touyserkan County in 2013

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
IRCT
Registry ID
IRCT201301306807N6
Enrollment
126
Registered
2013-07-17
Start date
2013-04-22
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: childbirth pain. Condition 2: anxiety of childbirth. Low back pain Generalized anxiety disorder

Interventions

Intervention 1: In aromatherapy group, 4 ml of citrus scents is stained with gas and attached to the collar of the patients. Every half hour, the prescription will be repeated. Intervention 2: In cont
Treatment - Drugs
Placebo
In aromatherapy group, 4 ml of citrus scents is stained with gas and attached to the collar of the patients. Every half hour, the prescription will be repeated.
In control group, 4 ml of normal saline is stained with gas, and every half hour, this is repeated.

Sponsors

Vice-Chancellor for Research Dept of School of Nursing and Midwifery Shahid Beheshti University of M
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 35 Years

Inclusion criteria

Inclusion criteria: Inclusion Criteria: be Iranian; be nulliparous; be at the age of 18-35 years old; have a singleton term pregnancy; fetal presentation should be vertex; onset of contractions should be spontaneous, and at the beginning of admission, have a 3 to 4-cm dilatation; appropriate pelvic position; estimated fetal weight should range from 2500 to 4000 gr; amniotic sac should be sound when admitting to the study; over the past 8 hours, mother have not used analgesic medicines; have no known liver, gallbladder, and respiratory disease records in her file; according the file, have no complication during pregnancy such as pre-eclampsia, bleeding and infection; according to her, have not olfactory problems; according to her, not sensitive to herbal medicines. Exclusion criteria: emergency cesarean before completing the study; sensitive to citrus scents and non-tolerance during the study term; obstetric complications such as vaginal bleeding during the study; analgesic intake during the study.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Intensity of pain. Timepoint: before and after intervention in 3-4, 5-7, and 8-10 dilatations. Method of measurement: Numeric Rating scale Ruler.;Anxiety. Timepoint: before and after intervention in 3-4, 5-7, and 8-10 dilatations. Method of measurement: Speilberger checklist.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMasoumeh Namazi

School of Nursing and Midwifery, Shahid Beheshti University of Medical Sciences

masnamazi@yahoo.com+98 81 1825 5724

Outcome results

None listed

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