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Clinical Trials in Turkey / NCT06535230
Recruiting Not applicable

Anesthesia Induction with the Target-controlled Infusion of Propofol in High-risk Patients

NCT06535230 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2024-08-30
Last updated
2025-02-03

Condition(s) studied

AnesthesiaHemodynamic Instability

Investigational drug(s) / intervention(s)

Manual anesthesia inductionAnesthesia induction with Target controlled infusions (TCI)Hemodynamic monitoring with pressure recording analytical method (PRAM)

Manual anesthesia induction: In manual anesthesia induction, anesthetic agents are administered at a fixed dose and rate adjusted according to the patient's weight

Anesthesia induction with Target controlled infusions (TCI): Target controlled infusion (TCI) system aims to reach the theoretically targeted blood or brain concentration of anesthetic agents based on the patient's age, weight, and height, with computer-assisted algorithms.

Hemodynamic monitoring with pressure recording analytical method (PRAM): The pulse contour device MostCare (Vytech, Vygon, Padova, Italy) provides functional hemodynamic monitoring using the pressure recording analytical method.

Study summary

The purpose of this study is to compare the risk of hypotension following induction of anesthesia in high-risk patients (American Society of Anesthesiologists risk scores III and IV) using target-controlled infusion (TCI) of propofol versus standard manual induction of anesthesia. Our previously published study compared TCI and manual induction of anesthesia in a general patient population and found that hypotension developed less with TCI induction. This study is a continuation of the other study and will be conducted in high-risk patients.

Eligibility

Sex
ALL
Min age
18 Years
Max age
100 Years
Healthy volunteers
No
Inclusion Criteria: * Patients with the American Society of Anesthesiology physical status 3-4 * Underwent major elective surgery * Required intra-arterial blood pressure monitoring before induction. Exclusion Criteria: * Under 18 years of age * Patients with the American Society of Anesthesiology physical status 1-2 * Arrhythmia (atrial fibrillation, frequent premature beat) * Severe valvular heart disease * Morbid obesity * Intubation difficulty * Drug addiction * Treatment with opiates * Pregnancy * Emergency surgery

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Acibadem Altunizade Hospital Istanbul Turkey (Türkiye) Recruiting

More Acibadem University trials in Turkey

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06535230 on ClinicalTrials.gov ↗ ← All trials in Turkey