Single spontaneous delivery. Single spontaneous delivery
Conditions
Interventions
Intervention 1: The first group of 25 patients who received spinal anesthesia. Intervention 2: The second group of 25 patients who received an epidural.
Treatment - Drugs
The first group of 25 patients who received spinal anesthesia.
The second group of 25 patients who received an epidural.
Sponsors
Semnan University of Medical Sciences
Eligibility
Sex/Gender
Female
Inclusion criteria
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
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Analgesia. Timepoint: Before and after the intervention to end delivery process. Method of measurement: Numeric Rating Pain Scale. | — |
Secondary
| Measure | Time frame |
|---|---|
| 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. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactForozeshfard Mohammad
Semnan University of Medical Sciences
Outcome results
None listed