Not Yet Recruiting PHASE4 INTERVENTIONAL 3-arm
NCT06715657
Effect of Propofol Administration Time on the Incidence and Severity of Intrathecal Morphine-induced Pruritus in Parturient Undergoing Elective Cesarean Delivaries
Effect of Propofol Administration Time on the Incidence and Severity of Intrathecal Morphine-induced Pruritus in Parturient Undergoing Elective Cesarean Delivaries: A Prospective, Randomized, Comparative Controlled Study
Sponsor: Assiut University
Conditions
Cesarean Section
Interventions
Morphine intrathecal propofol
Updated 1 time since 2025 Last updated: Dec 3, 2024 Started: Dec 1, 2024 Primary completion: Dec 1, 2026 Completion: Jan 1, 2027
This information is for research purposes only and is not medical advice. Consult a healthcare provider before making any medical decision.
A PHASE4 clinical study on Cesarean Section, this trial is actively recruiting participants. The trial is conducted by Assiut University and has accumulated 1 data snapshot since 2024. Longitudinal tracking of this trial contributes to a broader understanding of treatment development timelines.
Status Flow
Change History
1 version recorded Not Yet Recruiting — PHASE4
[monthly]
Eligibility Summary
No eligibility information available.
Contact Information
Sponsor contact:
- Assiut University
Data source: Assiut University
For direct contact, visit the study record on ClinicalTrials.gov .
Study Locations
No location information available.