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Comparison of the effect of Entonex gas with Bl32 and sp6 pressure points on labor pain, labor stages and labor outcomes

Comparison of the effect of Entonex gas with Bl32 and sp6 pressure points on labor pain, labor stages and labor outcomes in primiparous women

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20230717058818N1
Enrollment
90
Registered
2023-08-21
Start date
2023-08-11
Completion date
Unknown
Last updated
2023-10-16

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

Conditions

Labor duration, labor pain and maternal and fetal complications after delivery.

Interventions

Intervention 1: Intervention group: entonex.Until the client learns how to use the Entonx mask and capsule and identify uterine contractions, the training will continue, and Entonx gas with a mask wil

Sponsors

Ilam University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 35 Years

Inclusion criteria

Inclusion criteria: Consent to participate in the study Having literacy Singleton pregnancy Gestational age 37 to 41 weeks Fetal cephalic status Women being in the active phase Not suffering from mental disorders No Anatomical disorders Not using other methods of anesthesia Not using oxytocin to induce and strengthen labor

Exclusion criteria

Exclusion criteria: Multiple pregnancy Mother's chronic illness Skin diseases such as eczema high risk pregnancy

Design outcomes

Primary

MeasureTime frame
Labor progress. Timepoint: 4 cm dilatation, every one hour during intervention and after delivery. Method of measurement: Checklist of Duration of Labor Stages.;Labor pain. Timepoint: one hour during labor. Method of measurement: Ten Degree Visual Analogue scale.;Maternal and Neonatal Outcomes. Timepoint: After giving birth and the day after giving birth. Method of measurement: Checklist of Maternal and Neonatal Outcomes.

Secondary

MeasureTime frame
Maternal and neonatal complications after delivery. Timepoint: Before birth and one day after delivery. Method of measurement: Checklist of maternal and newborn outcomes designed by the researcher.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactShaghayegh Gheitasiilami

Ilam University of Medical Sciences

gheitasi-s@medilam.ac.ir+98 84 3333 3333

Outcome results

None listed

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