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PropofolTCINCT07259291

Minto and Eleveld Remifentanil Target Controlled Infusion (TCI) Models: a Clinical Comparison

An observational study of Propofol and Anesthesia Brain Monitoring, run by University of Padova at 1 site in Italy.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

Remifentanil is commonly used as an opioid during general anesthesia. In recent years, several pharmacokinetic/pharmacodynamic (PK/PD) models for target-controlled infusion (TCI) have been developed, with the Eleveld model being one of the most recent and designed for broad applicability. Read more about this study

Who is it for?
Ages 18 to 80 years, women only
How many people
100 participants
Where
1 siteItaly
Study dates
25 Nov 2025to 30 Dec 2026
Phase
Observational
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 80 years
  • Women only
  • Adult, Older adult

Study population: Women undergoing brast cancer surgery with general anesthesia with Propofol and Remifentanil TCI, will be recruited

Who may be able to join

  • Undergo general anaesthesia with Targeted Controlled Infusion of Propofol (Eleveld model) and Remifentanil (Minto or Eleveld model)

Who cannot join

  • Neurological disease
  • Psychiatric disease

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Italy1 site, 1 recruiting
  • ULSS2 Marca Trevigiana

    Treviso, 31100

    Federico Linassi, MD, 0422322440, federico.linassi@gmail.com

    Recruiting

Other trials in Italy

About this study

Official title: Minto and Eleveld Remifentanil Target Controlled Infusion (TCI) Models: a Clinical Comparison Through qNOX and ANIi Reactions to Post-tetanic Count

Remifentanil is commonly used as an opioid during general anesthesia. In recent years, several pharmacokinetic/pharmacodynamic (PK/PD) models for target-controlled infusion (TCI) have been developed, with the Eleveld model being one of the most recent and designed for broad applicability.

The aim of this study is to compare the Eleveld TCI model with the routinely used Minto model, in order to evaluate potential differences in the predicted effect-site concentrations (CeR) required to achieve equivalent analgesia levels, as measured by qNOX (CONOX monitor) and the Analgesia Nociception Index (ANI). Post-Tetanic Count (PTC) was also assessed during the maintenance phase to investigate possible differences in nociceptive index responses between the two TCI models.

Read the detailed description

Remifentanil is a short-acting synthetic opioid frequently used as part of balanced general anesthesia due to its favorable pharmacokinetic profile, which includes rapid onset, short context-sensitive half-time, and predictable elimination. These properties make it ideal for administration via target-controlled infusion (TCI), allowing anesthesiologists to maintain a desired effect-site concentration (Ce) with high precision.

Over the past two decades, several pharmacokinetic/pharmacodynamic (PK/PD) models have been developed to guide TCI of remifentanil. Among these, the Minto model has been widely adopted in routine clinical practice. It was originally derived from data collected in healthy volunteers and incorporates covariates such as age, weight, height, and sex. However, its applicability across broader patient populations has been questioned, particularly in individuals outside the demographic or physiological range of the original dataset.

More recently, the Eleveld model has been introduced as a general-purpose model for remifentanil TCI. It was developed using a large pooled dataset covering a wide range of patient types, including pediatric, adult, and elderly individuals. This model aims to offer more accurate and consistent predictions of drug concentrations and effects across diverse clinical scenarios.

The primary aim of this study is to compare the Eleveld and Minto models with respect to the effect-site concentration (CeR) of remifentanil required to achieve comparable levels of intraoperative analgesia. Analgesia was assessed using two objective nociception monitors: the qNOX index (derived from the CONOX monitor) and the Analgesia Nociception Index (ANI). These indices provide continuous, real-time information on the balance between nociceptive stimulation and the analgesic effect, allowing for a quantitative comparison between the two models.

To further explore the analgesic efficacy and responsiveness under each model, investigators introduced controlled nociceptive stimuli during the maintenance phase of anesthesia. Specifically, the Post-Tetanic Count (PTC) stimulation was applied during anesthesia maintenance to serve as a standardized noxious input. The response of the analgesia monitoring indices (qNOX and ANI) to this stimulus was analyzed, enabling the assessment of how each TCI model modulates analgesic depth in the face of a defined nociceptive challenge.

By comparing the CeR values, the baseline and post-stimulus nociception indices, and their temporal patterns under the two models, this study aims to determine whether the Eleveld model offers any clinical or pharmacodynamic advantages over the traditional Minto model in guiding remifentanil administration during general anesthesia.

Keywords
Analgesia monitoring

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

Study groups in NCT07259291
Study groupRoleWhat they receive
Eleveld TCIPatients who received general anesthesia with Eleveld TCI model for Propofol and Remifentanil (this model was choosen at anesthesiologist's discretion)
Minto TCIPatients who received general anesthesia with Eleveld TCI model for Propofol and Minto TCI for Remifentanil (this model was choosen at anesthesiologist's discretion)

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Comparison between Concentration at the effector site of Remifentanil (CeR) during anesthesia maintenance

    Discover if there are differences between CeR of Eleveld and Minto TCI to aim at the same analgesic depth as measured by qNOX (40-60) and ANI (50-70)

    Measured: We will consider CeR, qNOX and ANI values during the periprocedural phase

Secondary outcomes (4)
  1. Comparison between qNOX and ANI reaction to noxious stimulation delivered by Post-tetanic count during maintenance of anesthesia

    Discover if there is indices increase (for qNOX) or decrease (for ANIi) after post-tetanic count stimulation during general anesthesia between the Minto and Eleveld TCI model for Remifentanil

    Measured: qNOX, ANIi will be recorded during the periprocedural phase

  2. Comparing the incidence of Postoperative Delirium (POD) at anesthesia emergence

    Discover if there are different POD rates detected by Confusion Assessment Method (CAM) between Eleveld or Minto TCI models. Higher POD probability with higher CAM scores

    Measured: CAM will be performed in Post Anesthesia Care Unit, 45 minutes after the end of surgery

  3. Comparing the incidence of pain at anesthesia emergence

    Discover if there are different Severe pain rates detected by Numeric Rating Scale (NRS) between Eleveld or Minto TCI models.Higher pain with higher NRS scores

    Measured: NRS will be performed in Post Anesthesia Care Unit, 45 minutes after the end of surgery.

  4. Comparing the incidence of cronic pain after 6 months from surgery

    Discover if there are different Severe pain rates detected by Numeric Rating Scale (NRS) between Eleveld or Minto TCI models.Higher pain with higher NRS scores

    Measured: NRS will be performed after 6 months from surgery

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted2 Dec 2025
  2. Study start25 Nov 2025
  3. Primary completion30 Dec 2026 (estimated)
  4. Study completion30 Dec 2026 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Case-control
Time perspective
Prospective
Enrolment
100 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07259291
Sponsor's protocol ID
RemiMAST
Acronym
TCI
Status last verified
Jun 2026
First submitted
29 Sep 2025
Last updated
8 Jun 2026
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Undecided

Questions about this trial

What is this clinical trial studying?

An observational study of Propofol and Anesthesia Brain Monitoring, run by University of Padova at 1 site in Italy.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 8 Jun 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Italy. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Each site lists its own contact: choose the nearest one under Trial locations. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Comparison between Concentration at the effector site of Remifentanil (CeR) during anesthesia maintenance (time frame: We will consider CeR, qNOX and ANI values during the periprocedural phase). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 8 Jun 2026.

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