Recall of cardioversion after procedural sedation with propofol

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

NL-OMON

Registry ID

NL-OMON23740

Enrollment

Registered

2014-09-15

Start date

2014-11-01

Completion date

Unknown

Last updated

2024-02-28

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

Conditions

Patiënts with persistent arrhythmias for which cardioversion is indicated

Interventions

NRS-painscore before, directly after and some days after cardioversion

Eligibility

Inclusion criteria

Inclusion criteria: Patients >18 years old, admitted for scheduled cardioversion of persistent arrhythmia

Exclusion criteria

Exclusion criteria: - An inability to understand the questions (eg, language problems) - Protein or soy intolerance - Chronic pain

Design outcomes

Primary

Measure	Time frame
The incidence of a recall in patients who underwent cardioversion and were sedated with propofol	—

Secondary

Measure	Time frame
The difference in NRS score (recall) directly after and some days after cardioversion	—

Contacts

Public ContactD.F.M. Winden, van

Resident Intensive Care MC Haaglanden

dfm@vanwinden.net-

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)