lowering labor pai

Phase 3

• Conditions: Delivery.; Pregnancy,childbirth and the puerperium? Single spontaneous delivery; o99-o00 ?

• Registration Number: IRCT201207182624N9
• Lead Sponsor: Vice chancellor for research , Tehran University of Medical Sciences.

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: 120

Inclusion Criteria

Inclusion criteria included: term singleton pregnancy; cephalic presentation and appropriate pelvis.
Exclusion criteria are: any systemic disorder like asthma; hypertension; diabetes; multiparity; any sign of fetal distress and fetal death; any vaginal bleeding more than labor show; and placenta previa ( low risk pregnancy).

Exclusion Criteria

Not provided

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
abor pain. Timepoint: 30 minutes. Method of measurement: VAS.

Secondary Outcome Measures

Name	Time	Method
Duration of labor. Timepoint: From the beginning of the active phase of labor till full dilatation ( active phase of the first stage) and from full dilatation ( 10 cm) till delivery of fetus( second stage ). Method of measurement: Minute.