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Efficacy of conducting acupuncture on intensity and duration of labor pain

A randomized clinical trial on comparison of efficacy of LI-4 and SP-6 acupuncture points and Sham acupuncture on intensity and duration of labor pain in pregnant women

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2013061310657N2
Enrollment
63
Registered
2015-07-26
Start date
2011-10-01
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

labour pain. Maternal care related to the fetus and amniotic cavity and possible delivery problems

Interventions

Intervention 1: Intervention1: The acupuncture was conducted in intervention group after initiation of the active phase of labor defined by cervical dilatation of at least 4 centimeters and uterine co
Treatment - Other
Intervention1: The acupuncture was conducted in intervention group after initiation of the active phase of labor defined by cervical dilatation of at least 4 centimeters and uterine contractions at le
Intervention 2: In the control group, sham acupuncture was performed by superficial contact of needles in the mentioned points (LI4 and Sp6).

Sponsors

Vice chancellor for research, Shiraz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 40 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: 1-Persian speaking women 2-maternal age 20 - 40 years old 3-nulliparity 4-singleton pregnancy 5-being healthy 6-37-42 weeks of gestational age 7-cephalic fetal presentation 8-mothers with normal healthy fetus 9-healthy mother with no underlying diseases such as overt diabetes, gestational diabetes and preeclampsia Exclusion criteria: 1-mothers who received analgesics prior to conducting intervention 2-mothers who needs emergency cesarean section

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Duration of labour. Timepoint: Immediately after intervention. Method of measurement: Questionnaire.;Severity of pain. Timepoint: Before and immediately after the intervention. Method of measurement: Visual analogue pain scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactNajmeh Maharlouei

Shiraz University of Medical Sciences

maharluei@sums.ac.ir+98 71 3230 9615

Outcome results

None listed

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