reducing labor pai

Phase 2

• Conditions: delivery.; Other obstetric conditions, not elsewhere classified; O00-O99

• Registration Number: IRCT2015090615338N3
• Lead Sponsor: Tehran University of Medical Science research

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 22 February 2018

Recruitment & Eligibility

• Status: Complete
• Sex: Female
• Target Recruitment: 90

Inclusion Criteria

primiparous women with physical and mental health patients in the active phase; the prediction of vaginal delivery with a normal history and physical examination by a medical team; The Midwifery no problems in accepting the views of abnormal embryos, multiple pregnancies, fetal macrosomia, and pelvic disproportion, polyhydramnios, olygohydramnios, preeclampsia, premature placental separation, placenta previa, fast delivery and uterine infections; with a singleton pregnancy, cephalic view; no risk of hypertension, diabetes and other medical disorders in pregnancy; No risk of skin diseases like eczema, and any wound in the hot bag and massage; Having spontaneous contractions.

Exclusion criteria: All mothers of the natural course of maternal or fetal Labor Start due to factors such as detachment, cord prolapse, fetal distress out or for any reason during the Labor Start out of the labor and require special care or have an emergency cesarean section; Lack of desire to continue participating in the study; Use of drugs such as oxytocin labor catalyst; Use of an analgesic such as pethidine.

Exclusion Criteria

Not provided

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Pain. Timepoint: Every 30 minutes. Method of measurement: Visual analogue of pain.