Sakarya University Training and Research Hospital, Department of Anesthesiology and Reanimation
Sakarya, Adapazari, Turkey (Türkiye)
NCT Number: NCT07197567
This observational study aims to evaluate the clinical applicability of the Equivalent Minimum Alveolar Concentration (eMAC) parameter during general anesthesia. eMAC is a recently developed index that combines the effects of both inhalational and intravenous anesthetics, providing a unified measure of anesthetic depth. While the traditional Minimum Alveolar Concentration (MAC) is widely used for inhalational agents, it does not reflect intravenous anesthetics or combined techniques such as Combined Intravenous and Inhalational Anesthesia (CIVIA).
In this study, adult patients undergoing elective surgery under general anesthesia will be observed. Standard clinical practice will not be altered. Demographic and clinical parameters, including eMAC, MAC, Bispectral Index (BIS), and hemodynamic variables, will be recorded at defined perioperative time points. No experimental drugs or additional procedures will be administered.
The primary aim is to investigate the correlation between eMAC and MAC values obtained during anesthesia. Secondary objectives include assessing the relationship between eMAC and BIS values, comparing eMAC, MAC, and BIS across different anesthetic techniques, and evaluating hemodynamic stability in relation to anesthetic depth.
The results of this study may contribute to a better understanding of eMAC and its potential role in clinical anesthesia practice.
Looking for future studies?
Notify Me18 year–65 year
All sexes
Observational
Sakarya, Adapazari, Turkey (Türkiye)
This is a prospective, observational study designed to evaluate the Equivalent Minimum Alveolar Concentration (eMAC) parameter during general anesthesia. eMAC is a composite index that incorporates the anesthetic effects of both inhalational agents and intravenous anesthetics, such as propofol and remifentanil, allowing assessment of anesthetic depth under combined techniques (CIVIA). While the traditional Minimum Alveolar Concentration (MAC) is well established for inhalational agents, its applicability is limited in cases where intravenous agents are administered. eMAC has been proposed as a more comprehensive measure, but clinical validation is lacking.
Adult patients (ages 18-65, ASA I-III) scheduled for elective surgical procedures under general anesthesia will be enrolled. No experimental interventions will be performed; anesthetic management will follow routine clinical practice. Participants will be observed in two groups, based on the anesthetic technique selected by the attending anesthesiologist.
Data collection will include demographic and baseline clinical variables, as well as anesthetic depth parameters (eMAC, MAC, Bispectral Index [BIS]) and hemodynamic variables (heart rate, mean arterial pressure, SpO₂). Measurements will be recorded at predefined time points: prior to induction (T0), 5 minutes after induction (T1), at the beginning of surgery (T2), at the midpoint of surgery (T3), and at the end of surgery (T4).
The primary outcome measure is the correlation between eMAC and MAC values obtained during anesthesia. Secondary outcome measures include the correlation between eMAC and BIS values, comparisons of eMAC, MAC, and BIS among different anesthetic techniques, and evaluation of hemodynamic stability in relation to anesthetic depth.
Statistical analysis will be performed using appropriate parametric or non-parametric tests, depending on the distribution of variables. Correlation analyses will be conducted using Pearson or Spearman methods, and the impact of demographic factors on eMAC will be explored using multivariate regression. A p-value <0.05 will be considered statistically significant.
The anticipated enrollment is 60 patients. The study is planned to start in September 2025 and is expected to be completed by November 2025. Findings may provide novel insights into the clinical validity of eMAC as a tool for assessing anesthetic depth, and its relationship with established parameters such as MAC and BIS.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Combination of an inhalational anesthetic (sevoflurane) and an intravenous opioid analgesic (remifentanil), both routinely used in clinical practice for maintenance of general anesthesia. These agents are administered according to standard of care, not as experimental interventions.
Combination of an inhalational anesthetic (sevoflurane), an intravenous anesthetic (propofol), and an intravenous opioid analgesic (remifentanil). These agents are routinely used together in clinical practice for combined intravenous-inhalational anesthesia (CIVIA). All drugs are administered according to standard of care, not as experimental interventions.
Time frame: From induction of anesthesia until the end of surgery (measured at five perioperative time points: prior to induction, 5 minutes after induction, at surgical incision, at the midpoint of surgery, and at the end of surgery)
To determine the relationship between eMAC values and conventional MAC values obtained from the anesthesia workstation.
Time frame: From induction of anesthesia until the end of surgery (measured at five perioperative time points: prior to induction, 5 minutes after induction, at surgical incision, at the midpoint of surgery, and at the end of surgery)
To assess the relationship between eMAC values and BIS as indicators of anesthetic depth.
Time frame: From induction of anesthesia until the end of surgery (measured at five perioperative time points: prior to induction, 5 minutes after induction, at surgical incision, at the midpoint of surgery, and at the end of surgery)
To compare anesthetic depth parameters obtained from the anesthesia workstation (eMAC and MAC values) and BIS monitor (BIS values) among patients managed with inhalational anesthesia, total intravenous anesthesia (TIVA), or combined intravenous-inhalational anesthesia (CIVIA).
Time frame: From induction of anesthesia until the end of surgery (measured at five perioperative time points: prior to induction, 5 minutes after induction, at surgical incision, at the midpoint of surgery, and at the end of surgery)
To evaluate heart rate (beats per minute) in relation to anesthetic depth parameters across study groups.
Time frame: From induction of anesthesia until the end of surgery (measured at five perioperative time points: prior to induction, 5 minutes after induction, at surgical incision, at the midpoint of surgery, and at the end of surgery)
To evaluate mean arterial pressure (mmHg) in relation to anesthetic depth parameters across study groups.
Time frame: From induction of anesthesia until the end of surgery (measured at five perioperative time points: prior to induction, 5 minutes after induction, at surgical incision, at the midpoint of surgery, and at the end of surgery)
To evaluate peripheral oxygen saturation (percentage, %) in relation to anesthetic depth parameters across study groups.
Sakarya University
Other
Evaluation of Equivalent Minimum Alveolar Concentration During General Anesthesia: An Observational Study
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.
Published trials that share one or more normalized conditions with this study.
NCT07280546
General Anesthesia, Intraoperative Monitoring
Taipei, Taiwan
View Trial DetailsNCT07040631
Breast Cancer, Breast Diseases
Yangsan, Gyeongsangnam-do, South Korea
View Trial DetailsNCT07199049
Eye Movements, General Anesthesia
Başakşehir, Istanbul, Turkey (Türkiye)
View Trial DetailsNCT06787196
Bone Cysts, Cysts
Selçuklu, Konya, Turkey (Türkiye)
View Trial Details