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Effect of acupressure on initiation of labor

Phase 2
Conditions
Cervical ripening and initiation of labor.
Spontaneous vertex delivery
Registration Number
IRCT2015042321904N1
Lead Sponsor
Vice Chancellor for Research, Shahid Beheshti University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
150
Inclusion Criteria

age of 18-35 years old? gestational age of 39-41 weeks based on LMP or ultrasound in first trimester? nulliparous women? single fetus with cephalic presentation? intact membrane? bishop score< 4? body mass index between 19/8 to 30? estimated fetal weight between ( 4000-2500 gr )? low risk pregnancy? not having sexual intercourse 24 hours before and up to end of the study? not use of any kind of chemical drug or herb to start labor for 36 hours before study
Exclusion criteria: discontinuing of the study by mother request? taking chemical or herbal drugs.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Cervical ripening. Timepoint: Before intervention,48 and 96 hours after intervation and at the time of hospitalization. Method of measurement: Examination.;Initiation of labor. Timepoint: Before intervention,48 and 96 hours after intervation and at the time of hospitalization. Method of measurement: Examination.
Secondary Outcome Measures
NameTimeMethod
During of second stage of labor. Timepoint: At last of study. Method of measurement: Questionnaire.;During of first stage of labor. Timepoint: At last of study. Method of measurement: Questionnaire.;Neonatal Apgar. Timepoint: At last of study. Method of measurement: Questionnaire.;Use of oxytocin. Timepoint: At last of study. Method of measurement: Questionnaire.;Type of delivery. Timepoint: At last of study. Method of measurement: Questionnaire.
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