40
Participants
Start Date
September 22, 2024
Primary Completion Date
December 20, 2024
Study Completion Date
March 31, 2025
Trodon® Hemofarm
Consent was taken from each patient prior to the enrollment into the study during the first interview and 2 ml of blood was withdrawal for the CYP2D6 genotyping. After the cesarean section surgery, each patient received one dose of 100mg/2ml Trodon® Hemofarm for treating the postpartum pain and the patients were monitored for 24 hours. Follow-up was performed for each enrolled patient in which the VAS score, blood pressure, heart rate, oxygen saturation and any new effects after 1 hour, 6 hours of tramadol administration were recorded. In addition, after 24 hours evaluations for nocturnal pain, dietary state and bowel movement were performed.
Hawler Medical University/ College of Medicine, Erbil
Elweyia Maternity Teaching Hospital
OTHER