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Clinical Trial Summary

The purpose of this study is to assess the driving and cognitive ability of gastrointestinal endoscopy patients at different time points after intravenous anesthesia (propofol for example), and to explore whether the driving and cognitive ability have a relationship with the blood concentration of propofol or not.


Clinical Trial Description

20-70 year-old volunteers who hold legitimate licenses were recruited to have gastroscopy or colonoscopy under intravenous anesthesia with propofol, and before endoscopy using driving simulator and NCT to measure patients' driving ability and cognitive function as a baseline, in the same way, assessing patients' driving ability and cognitive function after 2h, 4h of the endoscopy , meantime collecting blood samples and separating blood plasma, using HPLC (High Performance Liquid Chromatography) to measure blood concentration of propofol. ;


Study Design

Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Supportive Care


Related Conditions & MeSH terms


NCT number NCT02280148
Study type Interventional
Source Beijing Friendship Hospital
Contact
Status Completed
Phase N/A
Start date November 2013
Completion date March 2014

See also
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Completed NCT00559819 - Validation of Driving Simulator to Blood Alcohol Concentration Standards for Impaired Driving Phase 3
Recruiting NCT06303765 - Evaluating the Practice Resource for Driving After Stroke N/A