se of transcutaneous electrical nerve stimulation (TENS) to relieve labor pai

Not Applicable

• Conditions: abor pain.The study was conducted in healthy women belonging to the target population, volunteers of the intervention with the goal of reducing labor pain.Pregnancy, childbirth and the puerperium; Labor pain; O00-O99; C10.597.617.515

• Registration Number: RBR-2zgdgj
• Lead Sponsor: Faculdade de Medicina de Botucatu

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2017-12-26
• Last Update Posted: 29 May 2023

Recruitment & Eligibility

• Status: Recruitment completed
• Sex: Female
• Target Recruitment: Not specified

Inclusion Criteria

Parturients with single gestation; cephalic presentation; preserved fetal vitality; with gestational age greater than or equal to 37 weeks; presenting cervical dilation greater than or equal to 4 cm and less than or equal to 7 cm.

Exclusion Criteria

indication of cesarean section prior to labor; presence of fetal death or fetal malformation; parturients with severe pathologies (clinical and obstetrical); twin pregnancy; rupture of the ovary membrane; and the use of any pharmacological method were excluded. pain control; presence of dermatitis or any infection at the site of TENS electrodes.

Study & Design

• Study Type: Intervention
• Study Design: Not specified