ClinicalTrials.Veeva

Menu

Waiting Time in the Premedication Room on Anxiety

I

Istinye University

Status

Active, not recruiting

Conditions

Total Anesthetic Consumption

Treatments

Behavioral: total anesthetic consumption

Study type

Observational

Funder types

Other

Identifiers

NCT06477731
istinye erkan

Details and patient eligibility

About

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.

Enrollment

130 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

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

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems