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Comparison of the effects of Entonox and Transcutaneous Nerve Stimulation in labor pain

Comparison of the effects of Entonox and Transcutaneous Nerve Stimulation in labor pain

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201011295274N1
Enrollment
117
Registered
2010-12-29
Start date
2010-12-06
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

labor pain.

Interventions

Intervention 1: GROUP1: This group use the TENS device , which it,s electrodes put on the spine at the level of T10-L1 & S2-S4 . The patient turn on the device by beginning the uter
Prevention
GROUP1: This group use the TENS device , which it,s electrodes put on the spine at the level of T10-L1 & S2-S4 . The patient turn on the device by beginning the uterus contractions
Group 2- In this group the patient press a button on the mask to inhale Entonox while uterus contractions begin . She ends the inhalation by ceasing the contractions . Silent TENS i
Group 3- In this group the patients use both TENS & Entonox simultaneously

Sponsors

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

Eligibility

Sex/Gender
Female
Age
20 Years to 40 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Normal monofetus term pregnancy(37-42 weeks) , normal vaginal delivery , lack of request for epidoral anesthesia, head down position of fetus , uncomplicated pregnancy , less than 4 cm of cervix dilatation, age of mother between 20-40 years and satisfying of mother regarding awareness of the methods used in the study . Exclusion criteria: Multifetus pregnancy , history of diabetic mellitus , hypertension, dermal skin infections such as herpes zoster , epilepsy , cardiovascular diseases, pacemaker , coagulation disorders or other diseases of the mother , preterm delivery

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Pain intensity. Timepoint: 4 times: before intervention , at the dilatation of 4-6 - , 6-8 and 8-10 cm. Method of measurement: visual analogue scale.

Secondary

MeasureTime frame
Duration of first phase of delivery. Timepoint: dilatation of 4-10 cm. Method of measurement: vaginal examination regarding time measuring.;Nausea & vomiting. Timepoint: During labor and till 24 hours after delivery. Method of measurement: Inspection or asking the patient.;Apgar of newborn. Timepoint: Immediately after delivery. Method of measurement: by recording scores.;Use of analgesics. Timepoint: During labor. Method of measurement: Patient notes.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Soheila Samadzadeh , physiatrist

Farabi Hospital Kermanshah University of Medical Sciences

s_samadzadeh2000@yahoo.com+98 83 1826 0700

Outcome results

None listed

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