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The investigators designed a prospective randomized study to investigate the efficacy of intravenous (IV) preemptive versus preventive paracetamol on postoperative pain scores, patient satisfaction, total morphine consumption and the incidence of morphine-related side effects in patients undergoing cesarean section.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Group Preemptive (Group PE), | Active Comparator | Group I: i.V. paracetamol 1 g (100 ml) was given 30 min before induction of anesthesia. |
|
| Group Preventive (Group PV), | Active Comparator | Group II: i.V. paracetamol 1 g (100 ml) was given before the end of surgery. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Paracetamol was given intravenously in both group at different times | Drug |
|
| Measure | Description | Time Frame |
|---|---|---|
| Visual analog score (VAS) for pain | 24 hours |
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Inclusion Criteria:
38 weeks pregnancy, elective cesarean section.
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Exclusion Criteria:
morbid obesity, cardiac failure, depression.
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