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Pharmacotherapy Personalization of Cancer Patients

Pharmacotherapy Personalization of Cancer Patients Based on Modern Analytical and Computational Techniques

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04866498
Enrollment
22
Registered
2021-04-29
Start date
2016-07-01
Completion date
2021-03-31
Last updated
2021-04-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Head and Neck Neoplasms, Oncologic Patients

Keywords

Anesthesia, Intensive Care Units, Pharmacokinetics, Pharmacodynamics, Surgical patients, Analgosedation

Brief summary

Treatment personalization could ensure better outcome than standard procedures. It is particularly important in intensive care units where patients received many drugs and procedures. Their health status can change very fast. The oncologic patients treated in intensive care units are a special group of patients. Factors related to cancer influence extra their health status. The aim of this study is population pharmacokinetic-pharmacodynamic analysis drugs that are routinely used during an analgosedation in ICU oncologic patients. Analgosedation is monitored by drugs plasma concentration, the depth of sedation (bispectral index) and vital parameters like: systolic and diastolic blood pressure, mean arterial pressure, heart rate. Moreover, the TNM Staging System, biochemical parameters, The American Society of Anesthesiologists (ASA) physical status classification will be checked like potential factors influencing on pharmacokinetics and pharmacodynamics drugs used in the study.

Detailed description

The oncologic patients are qualified to head and neck tumor resection in general anesthesia. The anesthesia introduction is performed with single dose of midazolam, fentanyl, rocuronium and propofol/etomidate. Sevoflurane is used in anesthesia maintenance. Patients are transported to ICU after operation. Then they are kept for several hours in analgosedation. All used drugs are given by intravenous continuous infusion. Oxycodone is an analgesic component of analgosedation. Midazolam, dexmedetomidine and/or propofol are used as sedatives (2-3 drugs in every patient). Whole blood samples (2.0 ml) are collected during the study to measure drugs concentrations - 3-4 times during infusion, 5, 10, 15, 30, 60 minutes and 2, 4, 6 hours after the infusion cessation. Vital parameters and bispectral index are monitored during analgosedation and 6 hours after the infusion cessation and noted every 15-60 minutes.

Interventions

DRUGInfusion Intravenous

Sponsors

The Greater Poland Cancer Centre
CollaboratorOTHER
Medical University of Gdansk
CollaboratorOTHER
Poznan University of Medical Sciences
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* age over 18 years old, * qualifications to oncologic surgery, * needing of analgosedation in ICU after an operation

Exclusion criteria

* proven allergies to used in anesthetics or/analgosedation medicaments, * lack of written confirmed consent of a patient

Design outcomes

Primary

MeasureTime frameDescription
Measurement of the depth of sedation using bispectral indexfrom the beginning of analgosedation to 6 hours after analgosedationContinuous measurement of the depth of sedation using bispectral index during analgosedation in intensive care unit.

Secondary

MeasureTime frameDescription
Dexmedetomidine plasma concentrations [ng/ml]3-4 times during infusion, 5, 10, 15, 30, 60 minutes and 2, 4, 6 hours after the infusion cessationMeasurements of dexmedetomidine plasma concentrations \[ng/ml\] during and after analgosedation. Whole blood samples (2.0 ml) were collected according to the study protocol.
Midazolam plasma concentrations [ng/ml]3-4 times during infusion, 5, 10, 15, 30, 60 minutes and 2, 4, 6 hours after the infusion cessationMeasurements of midazolam and alfa-hydroxymidazolam plasma concentrations \[ng/ml\] during and after analgosedation. Whole blood samples (2.0 ml) were collected according to the study protocol.
Propofol plasma concentrations [ng/ml]3-4 times during infusion, 5, 10, 15, 30, 60 minutes and 2, 4, 6 hours after the infusion cessationMeasurements of propofol plasma concentrations \[ng/ml\] during and after analgosedation. Whole blood samples (2.0 ml) were collected according to the study protocol.
Oxycodone plasma concentrations [ng/ml]3-4 times during infusion, 5, 10, 15, 30, 60 minutes and 2, 4, 6 hours after the infusion cessationMeasurements of oxycodone and noroxycodone plasma concentrations \[ng/ml\] during and after analgosedation. Whole blood samples (2.0 ml) were collected according to the study protocol.
Diastolic blood pressurebefore the beginning of analgosedation, during analgosedation, up to 6 hours after analgosedationMeasurements of diastolic blood pressure during analgosedation in intensive care unit.
Heart ratebefore the beginning of analgosedation, during analgosedation, up to 6 hours after analgosedationMeasurements of heart rate during analgosedation in intensive care unit.
Mean arterial pressurebefore the beginning of analgosedation, during analgosedation, up to 6 hours after analgosedationMeasurements of mean arterial pressure during analgosedation in intensive care unit.
Systolic blood pressurebefore the beginning of analgosedation, during analgosedation, up to 6 hours after analgosedationMeasurements of systolic blood pressure during analgosedation in intensive care unit.

Countries

Poland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026