pain after cesarean section. Acute pain, not elsewhere classified
Conditions
Interventions
Intervention 1: Intervention group: Paracetamol 1 g (Exir CO., Iran) and Dexmedetomidine 0.2 µg/kg (Abureihan CO., Iran) soluted in 100 cc normal saline will be injected via analgesic pump (Kanak Tech
Sponsors
Ahvaz University of Medical Sciences
Eligibility
Sex/Gender
Female
Age
18 Years to 40 Years
Inclusion criteria
Inclusion criteria: Age between 18 to 40 years ASA Class I and II Candidate for elective cesarean section No drug allergies to dexmedetomidine, ketorolac and paracetamol Stable hemodynamics Consent to participate in the study
Exclusion criteria
Exclusion criteria: history of asthma history of bleeding or gastrointestinal ulcer severe liver disease
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Severity of Pain. Timepoint: The time of 2, 4, 8, 12 and 24 hours after the surgery. Method of measurement: Visual analog scale (VAS).;Hemodynamics changes (Systolic and diastolic blood pressure, heart rate). Timepoint: The time of 2, 4, 8, 12 and 24 hours after the surgery. Method of measurement: Mercury barometer. | — |
Secondary
| Measure | Time frame |
|---|---|
| Nausea and vomiting. Timepoint: The time of 2, 4, 8, 12 and 24 hours after the surgery. Method of measurement: presence of nausea and vomiting based on direct observation and patients report.;Intensity of patients' anxiety. Timepoint: The time of 2, 4, 8, 12 and 24 hours after the surgery. Method of measurement: Ramsey sedate score (1-6). | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactHamid Hajilari
Ahvaz University of Medical Sciences
Outcome results
None listed