MedPath

Effect Of Acupressure On Delivery

Not Applicable
Conditions
Severity of labor pain and Outcome of Delivery.
Delivery
O80-O84
Registration Number
IRCT2013120315643N1
Lead Sponsor
Vice chancellor for Research,Shiraz University Of Medical Science
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
78
Inclusion Criteria

inclusion criteria:primiparous women with single fetus,gestatioanal age between 37-40weeks,cephallic presentation?active phase(3-4)cm?no chronic illness(heart disses,blood pressure and diabetes)?no high risk pregnancy(preeclampsia,deceleration fetus activity.dead fetus,polyhydraminious.oligohydraminious,rubture of membarne over than 12 hours,infertility history)?no skin disses(exema)?no use of anesthesia.exclusion criteria:oxytocin induction?no normal heart rate that need to cesarean cection?problem in labor(cord prolapse...?lack of willingness to continue in every phase?areest need to cesarean cection.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Severity of labor pain. Timepoint: prior,immedietly,30minutes and 60minutes after intervention. Method of measurement: Visual Anlog Sccale.
Secondary Outcome Measures
NameTimeMethod
Duration of first and second stage of labor,episiatomy,perineum lacerationand neonate apgar. Timepoint: after the intervention. Method of measurement: quastionrie.
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