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Effect of Entonox gas compared with aromatherapy with Lavender on severity of labor pain

Effect of Entonox gas compared with aromatherapy with Lavender on severity of nulliparous women's labor pain

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20170906036081N2
Enrollment
60
Registered
2018-03-15
Start date
2018-01-21
Completion date
Unknown
Last updated
2018-03-26

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

Conditions

Severity of labor pain.

Interventions

Intervention 1: Intervention group: In the group using Entonox gas, people will be trained to breathe the mask on their mouths, starting with a 4 cm dilatation.They should tell their severity before a

Sponsors

The University of Kurdistan of Medical Science
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 35 Years

Inclusion criteria

Inclusion criteria: Women aged 35 to 18 can enter the study. Women who are nulliparous can participate in the study. The position of the embryo should be cephalic. Amenotypic fluid volume of the mother is normal. The last trimester of ultrasound has reported the normal weight of the fetus. According to the first day of the last menstruation, the gestational age is greater than 38 weeks. The mother is healthy in terms of respiratory system and smell.

Exclusion criteria

Exclusion criteria: Hypertension in mother . Diabetes in mother. The mother has thyroid problems. The embryo is macrosomal. The fetus is a IUGR or low birth weight . Long-term rupture of the curtains for more than 18 hours. Polyhydramnios Oligohydramnios Embryonic anomalies have been diagnosed. Mothers have allergies and respiratory illness. An uncontrollable heartbeat of the fetus is created in the lab. SPO2 mother is less than 95% People who have contraindications to Entonox gas, such as head trauma, head stiffness, severe asthma, need for medical interventions in labor, are excluded from the study.

Design outcomes

Primary

MeasureTime frame
Severity of labor pain. Timepoint: The severity of pain is measured in dilates 4-5, 6-7, 8-9, and 10 cm before and after the intervention. Method of measurement: Visual Analogue Scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMaedeh Sharghi Chalaki

The University of Kurdistan of Medical Science

maedeh.sharghi@muk.ac.ir+98 87 3323 5445

Outcome results

None listed

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