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The effects of trans-cutaneous electrical stimulation on labor pain

The effects of trans-cutaneous electrical nerve stimulation ( Interferential current (IFC))in comparison with sham IFC on labor pain among nulliparous women

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20140811018760N5
Enrollment
60
Registered
2019-08-16
Start date
2019-09-23
Completion date
Unknown
Last updated
2019-10-07

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

Conditions

labor. Single spontaneous delivery

Interventions

Intervention 1: Intervention group: In this group, 30 to 45 minutes of electrical stimulation were obtained using a multistimulator (X735 Novin medical engineering company) at the start of the active

Sponsors

Tabriz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 45 Years

Inclusion criteria

Inclusion criteria: Primiparity one fetus Gestational age 37 -42 Early stage of active phase(dilation 4cm) Cephalic presentation of fetus

Exclusion criteria

Exclusion criteria: mother heart disease mother Diabetes mother High blood pressure Pre-eclampsia HELP syndrome Any skin problems in where electrodes will be located unwillingness to use electrical stimulation

Design outcomes

Primary

MeasureTime frame
Pain severity. Timepoint: The pain will be evaluated in several stages in both groups; first, before interventions and care, immediately after intervention, then every hour until the second stage of delivery, and at the end one hour after the delivery. Method of measurement: It will be measured using the Visual Analog Scale (VAS).;Duration of the active stage of labor. Timepoint: We will measure the time from the start of the active phase (reaching dilatation to 4 cm) to the end of the active phase (dilatation reaches 8 cm). Method of measurement: The duration will be determined from partography.

Secondary

MeasureTime frame
Frequency of satisfactory labor progress. Timepoint: during the active phase of labor will be determined. Method of measurement: It will be determined by examining the amount of dilatation of the cervix by vaginal examination, the fetal head descending , and the characteristics of uterine contractions by using partography.;The frequency of using sedative medications. Timepoint: From the start of interventions to an hour after the completion of labor. Method of measurement: The amount of its using dose will be recorded in the partography.;Frequency of need for oxytocin injection. Timepoint: From the beginning of the interventions to the end of labor. Method of measurement: The use or non-use of oxytocin will be recorded in the form of a partograghy and, if used, the number of drops per minute will be recorded in the partography.;1st and 5th minute Apgar Score. Timepoint: The first and fifth minutes after birth will be checked. Method of measurement: The Apgar score is obtained using the Apgar score table.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactFariba Ghaderi

Tabriz University of Medical Sciences

ghaderif@tbzmed.ac.ir+98 41 3334 5121

Outcome results

None listed

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