The effect of pre-procedure anxiety on sedative requirements for sedation during upper gastrointestinal endoscopy

Not Applicable

Completed

• Conditions: Anxiety and sedative requirements; Anaesthesiology - Anaesthetics; Mental Health - Anxiety; Oral and Gastrointestinal - Normal oral and gastrointestinal development and function

• Registration Number: ACTRN12615000369527
• Lead Sponsor: Konya Training and Research Hospital

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2015-04-22
• Last Update Posted: 13 January 2020

Recruitment & Eligibility

• Status: Completed
• Sex: All
• Target Recruitment: 300

Inclusion Criteria

Scheduled for elective upper gastrointestinal endoscopy.

ASA physical status I and II.

Exclusion Criteria

Patients with a history of any upper gastrointestinal surgery
A history of a psychiatric disease
Insufficient gastric preparation
A predicted difficult airway or allergy to propofol.
Non-elective patients.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Doses of propofol during endoscopy procedure.[Total doses of propofol (mg), (mg/kg) and mg/kg/min during endoscopy procedure.]

Secondary Outcome Measures

Name	Time	Method
Total procedure time[The time between the start and the end of endoscopy procedure];Satisfaction of patients<br><br>[Evaluation will be done after the procedure with a scale between 0-10 (10 point Likert Scale)];Satisfaction of endoscopists[Evaluation will be done after the procedure with a scale between 0-10 (10 point Likert Scale)]