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Clinical Trial 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)


Clinical Trial 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- In both groups, blood will be withdrawn to assess the possible effect of these medications on stress by measuring the following parameters: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 Design


Related Conditions & MeSH terms


NCT number NCT03143933
Study type Interventional
Source Cairo University
Contact May M Abdalla
Phone (002) 01002662985
Email mayezzeldin@miuegypt.edu.eg
Status Recruiting
Phase Phase 2/Phase 3
Start date July 2016
Completion date September 2017

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