Viewing Study NCT03143933


Ignite Creation Date: 2025-12-25 @ 2:47 AM
Ignite Modification Date: 2026-03-03 @ 12:35 AM
Study NCT ID: NCT03143933
Status: UNKNOWN
Last Update Posted: 2017-05-08
First Post: 2017-04-22
Is NOT Gene Therapy: True
Has Adverse Events: False

Brief Title: Comparison Between IV Propofol and Propofol/ Fentanyl Anesthesia on Patients Stress Response
Sponsor: Cairo University
Organization:

Study Overview

Official Title: Comparison Between IV Propofol and Propofol/ Fentanyl Anesthesia on Patients Surgical Stress Response Using BIS
Status: UNKNOWN
Status Verified Date: 2017-05
Last Known Status: RECRUITING
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: It is hypothesized that propofol, when used in general anesthesia (GA) influence patient's stress status and consequently affect stress response parameters. Hence, the objective of the presented research is to assess whether the propofol has anti-stress effect or not in patients undergoing surgeries that require GA and classified as The American Society of Anesthesiologists physical status 1 (ASA PS1)
Detailed Description: * Forty patients will be divided into two groups of patients (n=20 each), where in the first group anesthesia induction will be with propofol as a single agent, while patients in the second group will be anesthetized by propofol/fentanyl and the depth of anesthesia will be determined by BIS score and will be kept at 40-60.
* In both groups, blood will be withdrawn to assess the possible effect of these medications on stress by measuring the following parameters:

I- Hemodynamic indicators II- Catecholamines . III- Fasting blood glucose IV- Insulin level V- Cortisol VI- Vasopressin

VII- Cytokines:

Study Oversight

Has Oversight DMC:
Is a FDA Regulated Drug?:
Is a FDA Regulated Device?:
Is an Unapproved Device?:
Is a PPSD?:
Is a US Export?:
Is an FDA AA801 Violation?: