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Effects of jianjing with entonox on labour pain and duration of labour

The effect of acupressure on jyanjyng points and entonox on labour pain and delivery time in nulliparous women

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201312106807N11
Enrollment
174
Registered
2014-06-12
Start date
2013-10-29
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

Pain intensity and duration of delivery. Delivery

Interventions

Intervention 1: In the acupressure group, women receive the acupressure on the point jianjing. The 20-minute periodic acupressure on GB21 acupoint will performed at dilatation of 4-5, 6-7 and 8-10.(
Prevention
In the acupressure group, women receive the acupressure on the point jianjing. The 20-minute periodic acupressure on GB21 acupoint will performed at dilatation of 4-5, 6-7 and 8-10.( pressure on uter
In the entonox group, women receive the entonox at the beginning of the active phase of labor (cervical dilatation 4 cm) after learning how to use it. Labor pain will measured three times using a sub
In the control group,no intervention will be done. Labor pain will measured three times using a subjective labor pain scale. Length of delivery time will be calculated in first and second stage of la

Sponsors

Shahid Beheshti University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: Inclusion criteria: nulliparous women aged 18 to 35 years; be literate; singleton pregnant with gestational age 37 to 41 week; cephalic presentation; Iranian; tend to use analgesia (entonox gas or acupressure); women in the active phase of labor (3-4 centimeters cervical dilatation) or before; not suffering from poor mental health and anatomic (psychosis, schizophrenia, abnormalities of the uterus and pelvic); not having any head injury with some degree of lack of alertness, pneumothorax, and if such injury, atherosclerosis, poisoning and damage to the facial nerve; No risk to patients paced for chronic disease such as heart disease, pulmonary hypertension and diabetes; absence of high risk pregnancy such as gestational hypertension, decreased fetal movement, intrauterine growth restriction, fetal death, oligohydramnios and polyhydramnios and rupture of memberane more than 12 hours; a history of infertility; no risk of skin ailments such as eczema and infection of the skin surface. Exclusion criteria: any factor that would lead to a cesarean section; lack of desire to continue.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Pain intensity of delivery. Timepoint: Pain intensity in 4-5, 6-7 and 8-10 dillatation befor and after intervention. Method of measurement: visual-analogue scale.;Duration of delivery. Timepoint: ?First stage and second stage of labor. Method of measurement: Time.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSedigheh Amir Ali Akbari

Shahid Beheshti University of Medical Sciences

asa_akbari@yahoo.com+98 21 8820 2512

Outcome results

None listed

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