Ignite Creation Date:
2024-05-06 @ 7:55 PM
Last Modification Date:
2024-10-26 @ 3:17 PM
Study NCT ID:
NCT06188546
Status:
NOT_YET_RECRUITING
Last Update Posted:
2024-01-03
First Post:
2023-12-19
Brief Title:
Propofol for Prophylaxis of Morphine Induced Pruritis in Caesarean Section
Sponsor:
Assiut University
Organization:
Assiut University
Study Overview
Official Title:
Administration of Propofol for Prophylaxis of Intrathecal Morphine Induced Pruritus in Caesarean Section
Status:
NOT_YET_RECRUITING
Status Verified Date:
2023-12
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
the goal of this randomized clinical trial is to find the optimum sub hypnotic dose of iv propofol that prevents the incidence of itching induced from intrathecal morphine used in spinal anesthesia in caesarean section operation the main questions it aim to answer are the number of patients complained of pruritus in the first 24 hours post operative period and the severity of the pruritus participants will be divided into 4 groups 1st group receives 0 mg of propofol 2nd receives 10 mg 3rd receives 20 mg and the 4th receives 30 mg
Detailed Description:
None
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
True
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
False
Is an FDA AA801 Violation?:
None