Effects of Preoperative Operating Room Environment Presentation in Hypertensive Patients
Hypertension, Anxiety, Blood Pressure

About this trial
This is an interventional prevention trial for Hypertension focused on measuring Hypertensive patients, Introduction of operating room, Anxiety, Blood pressure
Eligibility Criteria
Inclusion Criteria:
- elective surgery
- informed consent,
- essential hypertension was diagnosed,
- Between the ages of 40-80,
- American Society of Anesthesiologists (ASA) class II-III
Exclusion Criteria:
- drug allergy,
- with a history of malignant hyperthermia,
- uncontrolled hypertension,
- cancer and psychological problems,
- patients with cardiac and endocrine diseases
- emergency surgery
Sites / Locations
- Van yuzuncu Yıl University, Dursun Odabas Medical Center
Arms of the Study
Arm 1
Arm 2
Active Comparator
No Intervention
Group IORE
Group NoIORE
This group will undergo the IORE procedure before surgery (operation). On the day of surgery, the patient will be brought to the operating room by the anesthesiologist. Hemodynamic data (blood pressure, pulse rate, respiratory rate, SpO2) will be measured at the service, preop unit and operating room. The anxiety level in the operating room will be measured by the ST-STAI scale.
The patient's hemodynamic data will be measured in the evening service before surgery. The patient will be brought to the operating room by the anesthesiologist on the day of surgery and hemodynamic data (blood pressure, pulse rate, respiratory rate, SpO2) will be measured in the preop unit. The hemodynamic data and the ST-STAI scale will measure the anxiety level in the operating room.