The effect of varying remifentanil infusion rates on target controlled infusion propofol concentrations necessary to maintain anaesthesia as assessed by bi-spectral index

Status

Completed

Phases

Phase 4

Study type

Interventional

Source

ANZCTR

Registry ID

ACTRN12605000269639

Enrollment

Registered

2005-09-02

Start date

2004-12-10

Completion date

Unknown

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

Interventions

Remifentanil and propofol at induction of anaesthesia.

Study design

Allocation

Randomised controlled trial

Intervention model

Single group

Primary purpose

Treatment

Masking

Blinded (masking used)

Eligibility

Sex/Gender

All

Age

25 Years to 60 Years

Healthy volunteers

Inclusion criteria

Surgery under general anaesthesia.

Exclusion criteria

Pregnant and breastfeeding women, severe ischaemic heart disease, severe hypovolaemia, allergy to propofol or egg, emergency surgery, current opioid, benzodiazepine or high alcohol use.

Outcome results