BIS monitoring and depth anaesthesia for cardioversion

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

ISRCTN

Registry ID

ISRCTN90337900

Enrollment

Registered

2007-09-28

Start date

2006-11-08

Completion date

Unknown

Last updated

2017-10-30

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

Conditions

Surgery: Anaesthesia Surgery Anaesthesia

Interventions

BIS monitoring vs standard treatment

Eligibility

Inclusion criteria

Inclusion criteria: Patients undergoing elective day case cardioversions for cardiac arrhythmias

Exclusion criteria

Exclusion criteria: Any patient not willing to consent or not able to consent, with history of malignant hyperthermia or hypersensitivity to propofol

Design outcomes

Primary

Measure	Time frame
Optimisation of depth of anaesthesia	—

Secondary

Measure	Time frame
To assess appropriateness of using BIS monitor when anaesthetising patients for cardioversion	—

Countries

United Kingdom

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026