postoperatve pain after cesarean section. Other complications of obstetric surgery and procedures
Conditions
Interventions
Intervention 1: In the study group paracetamol 1 g( volume =6.7ml) into 100 ml normal saline during 15 min, 20 min before the end of operation is infused. Intervention 2: In the placebo group 100 ml
Treatment - Drugs
In the study group paracetamol 1 g( volume =6.7ml) into 100 ml normal saline during 15 min, 20 min before the end of operation is infused.
In the placebo group 100 ml normal saline alone during 15 min, 20 min before the end of operation is infused.
Sponsors
Women's Reproductive Research Center, Tabriz University of Medical Sciences
Eligibility
Sex/Gender
Female
Age
18 Years to 40 Years
Inclusion criteria
Inclusion criteria: Inclusion criteria: Term parturients; Parturients with over 18 years; Parturients undergoing elective cesarean section with spinal anesthesia. Exclution criteria: To have a contraindication for spinal anesthesia; To have allergy to local anesthetics; Patients with mental disorders; Patients with organic dysfunctions; Previous chronic pain; Rased hepatic enzyms.
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pain. Timepoint: PACU, every 1 hour until 4 hours and then every 4 hours until 24 hours after operation. Method of measurement: Visual analogue scale (VAS) from 0 (without pain) to 10 (severe and intolerable pain). | — |
Secondary
| Measure | Time frame |
|---|---|
| Analgesic requirements. Timepoint: PACU, every 1 h until 4 h and then every 4 h until 24 h after operation. Method of measurement: Injection number and injection dose in mg. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactDr. Simin Atashkhoyi
Tabriz University of Medical Sciences
Outcome results
None listed