Epidural analgesia with two drugs, Bupivacaine and Rupivacaine.
Conditions
Interventions
Intervention 1: Intervention group:In the first group, after obtaining informed consent, 56 pregnant mothers with natural epidural analgesia (epidural analgesia) are contracted with bupivacaine. The p
Sponsors
Arak University of Medical Sciences
Eligibility
Sex/Gender
Female
Inclusion criteria
Inclusion criteria: Mothers with one fetus Pregnant mothers who are candidates for vaginal delivery (Physiological delivery) Nullipar pregnant mothers are candidates for vaginal delivery Pregnant women referring to Taleghani Hospital with informed consent to participate in the study. Mothers with ASA grade one and two Pregnant mothers between the weeks 37-42 Who are perfectly pregnant Pregnant mothers who are candidates for vaginal delivery, who are satisfied with epidertal analgesia
Exclusion criteria
Exclusion criteria: Patients in the epidural group who undergo epidural block failure after an epidural analgesia. Pregnant mothers who are candidates for cesarean section for emergency reasons (such as placental abruption, umbilical cord prolapse, etc.).
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Average cesarean section. Timepoint: After intervention, observing the progression of labor and the occurrence of problems requires intervention. Method of measurement: Examination.;Average active delivery time. Timepoint: After the intervention, when the cervical dilatation reaches 4 to 8 centimeters. Method of measurement: Examination.;Average duration of second stage of labor. Timepoint: After the intervention, from the beginning of the full dilation of the uterus until the birth of the baby. Method of measurement: Examination.;The average satisfaction of the patient. Timepoint: 2 hours after intervention. Method of measurement: Based on satisfaction checklist.;Number of use of labor aid tool. Timepoint: Up to 3 hours after intervention. Method of measurement: Number.;Mean Apgar score of 1 and 5 minutes. Timepoint: After the intervention, 1 and 5 minutes after childbirth. Method of measurement: Apgar score check list.;Average motor blocking effect. Timepoint: After intervention, up to 2 hours after childbirth. Method of measurement: Scoring patient in the checklist. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactNarges Anousheh
Arak University of Medical Sciences
Outcome results
None listed