post operative pain. Acute pain
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Inclusion criteria: ASA class I and II, age between 20 and 40 years old, scheduled to undergo Cesarean Section Exclusion criteria: Receiving analgesics or corticosteroids drugs, presence of contraindication to regional anesthesia, known hypersensitivity to the study drugs or if having any history of cardiac, respiratory, neuromuscular, Hepatic or renal disease, unwilling to participate
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Severity of pain. Timepoint: 4, 6, 12, 24 h after operation. Method of measurement: VAS-consisting of 100 mm line with 0 = no pain and 100 = worst possible pain. | — |
Secondary
| Measure | Time frame |
|---|---|
| Number of used suppository. Timepoint: 24 hrs after surgery. Method of measurement: Asking from Patient.;Nausea and vomiting intraoperatively. Timepoint: At the end of the surgery. Method of measurement: Asking from Patient.;Nausea and vomiting postoperatively. Timepoint: 24 hrs after surgery. Method of measurement: Asking from Patient.;Headache after surgery. Timepoint: 24 hrs after surgery. Method of measurement: Asking from Patient.;Time to rescue analgesic drug for the first time. Timepoint: Whenever the VAS goes higher than 4. Method of measurement: Asking from Patient. | — |
Countries
Iran (Islamic Republic of)
Contacts
Zanjan University of Medical Sciences