Skip to content

Observational, prospective drug administration and physiological data collection during anaesthesia

Real time drug administration and physiological data collection during anaesthesia: observational study to evaluate the validity of current response surface models available in the literature

Status
Completed
Phases
Unknown
Study type
Observational
Source
ANZCTR
Registry ID
ACTRN12610000277044
Enrollment
160
Registered
2010-04-07
Start date
2010-04-23
Completion date
2010-10-01
Last updated
2020-01-13

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

Conditions

None listed

Brief summary

Pharmacological models have a variety of applications, including automated drug infusion pumps and human patient simulators. These applications often extrapolate models beyond the datasets in which they were developed, and the uses for which they were designed. As such, models require validation in new datasets to ensure adequate performance. Collection of drug administration and effect data can be used to validate drug dose – effect models. We will prospectively collect data from surgical cases at Auckland City Hospital. This will allow construction of an observational dataset from which current pharmacological models can be validated in our patient population.

Interventions

This is a prospective, observational study. We will collect physiological and anaesthetic data prospectively for anaesthetics completed at Auckland City Hospital in the next two years. Electronic anaesthetic records will be collected and physiological data, patient demographics, and any other routinely collected information will be extracted. Data from all physiological monitoring will be directly downloaded during the procedure. Please note: this will not alter standard patient care. Use of all

This is a prospective, observational study. We will collect physiological and anaesthetic data prospectively for anaesthetics completed at Auckland City Hospital in the next two years. Electronic anaesthetic records will be collected and physiological data, patient demographics, and any other routinely collected information will be extracted. Data from all physiological monitoring will be directly downloaded during the procedure. Please note: this will not alter standard patient care. Use of all standard and additional monitoring will remain at the discretion of the anaesthetist. In addition, software designed to accurately read and log drug infusion rates from automated Total Intravenous Anaesthesia (TIVA) pumps will collect drug bolus and infusion rate data directly.

Sponsors

Department of Anaesthesiology, University of Auckland
Lead SponsorUniversity

Eligibility

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

Inclusion criteria

Patients receiving general anaesthesia from six demographic groups will be studied: * Healthy Adults: 18 - 65 years; body mass index 18.5 - 25 (as defined by the World Health Organisation) * Cardiac bypass patients * Elderly, defined as age > 70 years * Overweight, body mass index > 30 * Those who receive total intravenous anaesthesia * American Society of Anesthesiologists (ASA) grade 3-4 patients undergoing emergency surgery

Exclusion criteria

Patients with neurological dysfunction, head trauma, opioid dependence and renal or hepatic co-morbidities will not be studied

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026