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Clinical Trials/ACTRN12610000447055
ACTRN12610000447055
Completed
Phase 4

To explore the effect during induction of anaesthesia of low dose intravenous premedication (co-induction) with a variety of drugs, on cardiac output and the dose of propofol required for loss of consciousness, in patients requiring insertion of arterial line for surgery

Christchurch Anaesthesia Education Trust0 sites80 target enrollmentJune 2, 2010
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ConditionsAnaestheticsCardiac output changesAnaesthesiology - Anaesthetics

Overview

Phase
Phase 4
Intervention
Not specified
Conditions
Anaesthetics
Sponsor
Christchurch Anaesthesia Education Trust
Enrollment
80
Status
Completed
Last Updated
6 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
June 2, 2010
End Date
TBD
Last Updated
6 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
Christchurch Anaesthesia Education Trust

Eligibility Criteria

Inclusion Criteria

  • •Surgery requiring insertion of arterial line,
  • •American Society of Anesthetist (ASA) rating 1,2 or 3

Exclusion Criteria

  • •Contra\-indication to propofol.
  • •Requirement for specific co\-induction drug, other than study drug.

Outcomes

Primary Outcomes

Not specified

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