drugset / Trial / NCT06715657

Effect of Propofol Administration Time on the Incidence and Severity of Intrathecal Morphine-induced Pruritus in Parturient Undergoing Elective Cesarean Delivaries

NCT06715657 ↗

Phase 4 Not yet recruiting 204 enrolled Assiut University
RandomizedParallel-groupQuadruple-blindTreatment

Summary

Our hypothesis suggests that Administration time of intravenous propofol may affect Pruritus incidence and severity that occur after intrathecal morphine in parturient undergoing elective cesarean section (CS). the aim of the study is to investigate effect of prophylactic administration of intravenous sub-hypnotic dose of propofol before intrathecal morphine compared with the administration after intrathecal morphine on intrathecal morphine-induced pruritus incidence and severity in parturient undergoing elective cesarean delivaries.

Timeline

Start
2024-12-01
Primary completion
2026-12-01
Completion
2027-01-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Propofol Small molecule 0.5 mg/kg Intravenous
Background Morphine Other / unclassified — Intrathecal

Indications

No indication recorded.