Waiting Time in the Premedication Room on Anxiety

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

ACTIVE_NOT_RECRUITING

Total Enrollment

130 participants

Study Classification

OBSERVATIONAL

Study Start Date

2024-06-20

Study Completion Date

2024-07-30

Brief Summary

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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.

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Detailed Description

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Conditions

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Total Anesthetic Consumption

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Interventions

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total anesthetic consumption

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.

Intervention Type BEHAVIORAL

Eligibility Criteria

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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

Exclusion Criteria

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

Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No