Cesarean.
Conditions
Interventions
Intervention 1: Intervention group: Patients referred for cesarean section. For spinal anesthesia of 0.5% bupivacaine hydrochloride (4 ml / 20 mg ampoule - Mylan made in France by Haupt Pharma Livron
Sponsors
Qazvin University of Medical Sciences
Eligibility
Sex/Gender
Female
Inclusion criteria
Inclusion criteria: All patients referred for cesarean section Lack of exclusion criteria
Exclusion criteria
Exclusion criteria: History of chronic pain and analgesic use, bleeding or coagulation disorder, peptic ulcer, renal or hepatic insufficiency and asthma, uterine atony, twins, placenta previa, Placental abruption, accreta placenta
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pain after cesarean section. Timepoint: Up to 24 hours after delivery. Method of measurement: Verbal Rating Scale. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactMohammad Mahdi Mir Nasseri
Qazvin University of Medical Sciences
Outcome results
None listed