postoperative analgesia. Pain, unspecified
Conditions
Interventions
Intervention 1: in group 1 paracetamol 33 mg/kg for 24 h(2g for 60 kg)and dexmedetomidine 0.15 microgram/kg/h (200 microgram) for 24h are used in total volume 100cc with normal saline and 4cc/h conti
Treatment - Drugs
in group 1 paracetamol 33 mg/kg for 24 h(2g for 60 kg)and dexmedetomidine 0.15 microgram/kg/h (200 microgram) for 24h are used in total volume 100cc with normal saline and 4cc/h continuous flow
group 2 ketorolac 1mg/kg (60 mg) for 24h and dexmedetomidine 0.15 microgram/kg/h (200 microgram) for 24h are used in total volume 100cc with normal saline and 4cc/h continuous flow
Sponsors
Iran University of Medical Sciences
Eligibility
Sex/Gender
Female
Age
18 Years to 38 Years
Inclusion criteria
Inclusion criteria: Inclusion criteria: Parturients aged between 18 and 38, elective cesarean section; American Society of Anesthesiologists (ASA) physical statuses grade I and II; Singed infomed consent; neuroaxial (spinal or epidural) anesthesia; Exclusion criteria: A history of opioid analgesic use or tranquilliser use; History of coagulopathy, Psychopatology; History of gastrointestinal problem too NSAID; American Society of Anesthesiologists (ASA) physical statuses grade more than II; Emergency cesarean section; age less than 18 and more than 38 years old; general anesthesia; dissatisfaction
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pain. Timepoint: 6,12,24 h post operatie. Method of measurement: VAS. | — |
Secondary
| Measure | Time frame |
|---|---|
| Parturient satisfaction. Timepoint: 24 h. Method of measurement: parturient expression.;Sedation,nausea vomiting dizziness,bleeding. Timepoint: 6 12,24,hour. Method of measurement: ramsy sedation scor ,parturient expression. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public Contactshiva nowruzinia
Iran University of Medical Science
Outcome results
None listed