Pain after cesarean section. Pain, not elsewhere classified
Conditions
Interventions
Intervention 1: Intervention group: Ropivacaine 5 mg/cc (Aburaihan pharmaceutical CO., Iran) with fentanyl 25 µg (Aburaihan CO., Iran) with volume of 4 mL will be injected for spinal anesthesia. Inter
Sponsors
Ahvaz University of Medical Sciences
Eligibility
Sex/Gender
Female
Age
17 Years to 45 Years
Inclusion criteria
Inclusion criteria: Age between 17 to 45 years old ASA Class I and II Candidate for elective cesarean section No allergies to fentanyl, sufentanil and ropivacaine no history of addiction Consent to participate in the study
Exclusion criteria
Exclusion criteria: Severe liver disease Need for general anesthesia
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Duration of analgesia. Timepoint: After entering the recovery room, then every 15 minutes until the first hour, then every hour for 12 hours. Method of measurement: The duration of analgesia is the time of performing spinal anesthesia to Visual analog scale (VAS) grade 3.;Systolic blood pressure. Timepoint: At the beginning of the study (before the intervention) and then every 5 minutes until end of recovery. Method of measurement: Mercury barometer.;Diastolic blood pressure. Timepoint: At the beginning of the study (before the intervention) and then every 5 minutes until end of recovery. Method of measurement: Mercury barometer. | — |
Secondary
| Measure | Time frame |
|---|---|
| Nausea after surgery. Timepoint: In the first 12 hours after surgery. Method of measurement: Presence of nausea based on direct observation and patients report.;Vomiting after surgery. Timepoint: In the first 12 hours after surgery. Method of measurement: Presence of vomiting based on direct observation and patients report. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactAtusa Ahmadi
Ahvaz University of Medical Sciences
Outcome results
None listed