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Spinal and epidural anesthesia with bupivacaine and pethidine in Painless Childbirth

Phase 2
Conditions
Single spontaneous delivery.
Single spontaneous delivery
Registration Number
IRCT2013060312701N5
Lead Sponsor
Semnan University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
50
Inclusion Criteria

The study group were all pregnant women who were candidate for the normal vaginal delivery and they had no underlying disease consists of heart disease and asthma.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Analgesia. Timepoint: Before and after the intervention to end delivery process. Method of measurement: Numeric Rating Pain Scale.
Secondary Outcome Measures
NameTimeMethod
Changes in blood pressure. Timepoint: From start to finish the process of intervention delivery. Method of measurement: Pressure gauge.;Nausea and vomiting. Timepoint: From start to finish the process of intervention delivery. Method of measurement: Nausea, and stomach contents during delivery.;Respiratory depression. Timepoint: From start to finish the process of intervention delivery. Method of measurement: Observational.
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