The Impact of CYP2D6 Polymorphism on Tramadol Pharmacodynamics

Active, not recruitingOBSERVATIONAL
Enrollment

40

Participants

Timeline

Start Date

September 22, 2024

Primary Completion Date

December 20, 2024

Study Completion Date

March 31, 2025

Conditions
Post-cesarean PainCYP2D6 PolymorphismTramadol Resistance
Interventions
DRUG

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.

Trial Locations (1)

40/0112

Hawler Medical University/ College of Medicine, Erbil

All Listed Sponsors
lead

Elweyia Maternity Teaching Hospital

OTHER

NCT06814652 - The Impact of CYP2D6 Polymorphism on Tramadol Pharmacodynamics | Biotech Hunter | Biotech Hunter