MIBG scintigraphy in patients with inherited monogenic electric heart diseases

MIBG scintigraphy in patients with inherited monogenic electric heart diseases - MIBG scintigraphy in inherited monogenic electric heart diseases

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

NL-OMON

Registry ID

NL-OMON31577

Enrollment

150

Registered

2008-07-01

Start date

2008-02-01

Completion date

Unknown

Last updated

2024-05-13

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

Conditions

heart rhythm disorders ventricular fibrillation

Interventions

None listed

Eligibility

Age

18 Years to 99 Years

Inclusion criteria

Inclusion criteria: mutations carriers of the following diseases: Long QT syndrome Brugada syndrome CPVT

Exclusion criteria

Exclusion criteria: pregnancy

Design outcomes

Primary

Measure	Time frame
Differences between symptomatic and asymptomatic patients within a group with regards to the proportion of patients with abnormal MIBG scintigram.	—

Countries

Netherlands

Outcome results