Waiting Time in the Premedication Room on Anxiety

Active, not recruiting

• Conditions: Total Anesthetic Consumption

• Registration Number: NCT06477731
• Lead Sponsor: Istinye University

Brief Summary

The primary purpose of the study is to determine the total anesthetic consumption required to reach the optimal depth of anesthesia (BIS 50) depending on the anxiety of the waiting period in the preoperative waiting room and the degree of anxiety.

Detailed Description

Not available

Basic Information
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Recruitment & Eligibility
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Study & Design
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Trial Locations

Study Timeline

• Status Verified: 2024-06
• Study Start: 2024-06-20
• Study First Submitted: 2024-06-22
• Study First Submitted QC: 2024-06-22
• Last Update Submitted: 2024-06-22
• Study First Posted: 2024-06-27
• Last Update Posted: 2024-06-27
• Primary Completion: 2024-07-25
• Study Completion: 2024-07-30

Recruitment & Eligibility

• Status: ACTIVE_NOT_RECRUITING
• Sex: All
• Target Recruitment: 130

Inclusion Criteria

• Being in the age group of 18 and over
• Being literate and able to communicate
• Individuals will have surgery in ENT, Urology, Brain Surgery, Orthopedics, General Surgery, Plastic Surgery, CVS and gynecology and obstetrics departments.
• Agreeing to participate in the research voluntarily

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Exclusion Criteria

• alcohol or drug use
• history of psychiatric illness
• central nervous system disease
• use of psychotropic medication
• pregnancy
• lack of vision, hearing

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Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
total anesthetic consumption	1 month	The primary purpose of the study is to determine the total anesthetic consumption required to reach the optimal depth of anesthesia (BIS 50) depending on the anxiety of the waiting period in the preoperative waiting room and the degree of anxiety.

Trial Locations

Locations (1)

Istinye Üniversity; 🇹🇷 Istanbul, Merkez Mahallesi, Turkey