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Changes in a composite variability index (CVI) and bispectral index (BIS) in response to standardized pain stimuli during propofol remifentanil infusion.

Changes in a composite variability index (CVI) and bispectral index (BIS) in response to standardized pain stimuli during propofol remifentanil infusion. - Composite variability index versus BIS

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON33289
Enrollment
120
Registered
2009-06-23
Start date
2009-07-01
Completion date
Unknown
Last updated
2024-05-06

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

Conditions

diepte van anesthesie tijdens operatie optimize anesthesia

Interventions

pseudo-steady-state concentrations of remifentanil and various steady state level of BIS as guided by propofol effect compartment controlled TCI (closed-loop). protocol blz.8

Sponsors

Universitair Medisch Centrum Groningen
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: All patients: Age > 18 years and

Exclusion criteria

Exclusion criteria: patient refusal weight less than 70% or more than 130% of ideal body weight, neurological disorder recent use of psycho-active medication, including alcohol.

Design outcomes

Primary

MeasureTime frame
Changes of the BIS and CVI after a standard pain stimulus during various steady-state effect-site BIS levels and remifentanil as calculated by the software program Rugloop II (Demed Engineering, Temse, Belgium). Continuous bilateral BIS values throughout the study period.

Secondary

MeasureTime frame
to compare the changes in other vital signs such as heart rate and blood pressure compared to CVI in response to a standardized noxious stimulus during various targeted pseudo-steady-state concentrations of remifentanil and various steady state level of BIS as guided by propofol effect compartment controlled TCI (closed-loop).

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)