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NCT Number: NCT07488182

Preoperative Carotid Doppler Ultrasound Parameters for Prediction of Post-Induction Hypotension in Elective Non-Cardiac Surgery

This prospective observational study aims to evaluate the predictive value of preoperative carotid Doppler ultrasound parameters, including carotid velocity-time integral (carotid VTI) and corrected carotid flow time (ccFT), for post-induction hypotension in adult patients undergoing elective non-cardiac surgery under general anesthesia. Hemodynamic instability during anesthesia induction is a common and clinically important problem associated with adverse perioperative outcomes. Carotid Doppler ultrasonography provides a rapid and non-invasive method for assessing hemodynamic status at the bedside. In this study, carotid Doppler measurements will be performed in the preoperative period and their association with post-induction hypotension will be analyzed. The results of this study may help identify patients at risk for hypotension and improve perioperative hemodynamic management.

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Key information

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Necmettin Erbakan University

Konya, Turkey (Türkiye)

Location contact

Engin Kılınç, Medical Doctor

SUB_INVESTIGATOR

Engin Kılınç, medical doctor

CONTACT

[email protected]

00 90 332 223 60 00

SULE ARICAN, Assoc. Prof.

PRINCIPAL_INVESTIGATOR

About this study

Post-induction hypotension (PIH) is a common hemodynamic complication during the induction of general anesthesia and is associated with increased risk of perioperative morbidity and mortality. Identifying patients at risk of developing hypotension before anesthesia induction may allow anesthesiologists to implement preventive strategies and optimize perioperative hemodynamic management.

Traditional static hemodynamic parameters are often insufficient to accurately assess intravascular volume status and cardiovascular reserve. Doppler ultrasound-based measurements have emerged as useful non-invasive tools for evaluating cardiovascular dynamics. Carotid Doppler ultrasonography, in particular, allows rapid bedside assessment of hemodynamic parameters such as carotid velocity-time integral (carotid VTI) and corrected carotid flow time (ccFT), which may reflect changes in stroke volume and preload responsiveness.

This prospective observational study aims to evaluate the ability of preoperative carotid Doppler parameters, including carotid VTI and corrected carotid flow time (ccFT), to predict the development of post-induction hypotension in adult patients undergoing elective non-cardiac surgery under general anesthesia. Carotid Doppler measurements will be performed during the preoperative period, and anesthetic induction will be conducted in accordance with the study protocol under standard monitoring conditions. Hemodynamic parameters will be recorded during the induction period, and the occurrence of post-induction hypotension will be documented.

The primary objective of this study is to determine the predictive performance of carotid VTI and corrected carotid flow time for post-induction hypotension. Secondary analyses will explore the relationship between Doppler-derived hemodynamic parameters and perioperative hemodynamic changes. The findings of this study may contribute to improving perioperative risk stratification and guiding individualized hemodynamic management strategies.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Adult patients aged 18-65 years

American Society of Anesthesiologists (ASA) physical status I-II

Scheduled for elective non-cardiac surgery under general anesthesia

Planned endotracheal intubation

Ability to provide written informed consent

Exclusion criteria

Refusal to participate in the study

Planned emergency surgery

Planned cardiac surgery

Presence of carotid artery stenosis greater than 50%

Moderate to severe valvular heart disease

Presence of atrial fibrillation or significant arrhythmia

Advanced heart failure

Preoperative hypotension or hemodynamic instability

Inability to obtain reliable ultrasonographic measurements

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Treatment and study plan

Primary outcomes

  1. Post-induction hypotension

    Time frame: From anesthesia induction until 10 minutes after tracheal intubation or until the start of surgery, whichever occurs first.

    Occurrence of post-induction hypotension after anesthesia induction, defined as either a decrease in mean arterial pressure (MAP) of ≥30% from baseline or a MAP <65 mmHg sustained for at least 1 minute.

Secondary outcomes

  1. Predictive performance of carotid Doppler parameters

    Time frame: From the initiation of anesthetic induction until 10 minutes after tracheal intubation or until surgical incision, whichever occurs first.

    Diagnostic accuracy of preoperative carotid Doppler parameters (carotid VTI and corrected carotid flow time [ccFT]) for predicting post-induction hypotension, including area under the receiver operating characteristic curve (AUC), sensitivity, specificity, and optimal cut-off values.

Study contacts

Contact information is provided by the study sponsor or research team.

Engin Kılınç, Medical Doctor

CONTACT

[email protected]

00 90 332 223 60 00

Sponsors and collaborators

Lead sponsor

Necmettin Erbakan University

Other

Registry information

Official study title

The Value of Preoperative Carotid Doppler Ultrasonography Parameters in Predicting Post-Induction Hypotension in Patients Undergoing Elective Non-Cardiac Surgery

Important dates

Study start
2026
Primary completion
2027
Study completion
2027
First posted
Mar 23, 2026
Registry last updated
Mar 23, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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