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Echocardiography During Ajmaline Test

Dynamicity of Echocardiography During Ajmaline Test

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03491475
Enrollment
100
Registered
2018-04-09
Start date
2018-03-26
Completion date
2019-05-31
Last updated
2018-04-09

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

Conditions

Brugada Syndrome

Keywords

Ajmaline test

Brief summary

In this study the investigators analyse echocardiographic images before and during Ajmaline test. The purpose is to know if any echocardiographic modifications are present during either negative or positive Ajmaline testing.

Detailed description

The diagnosis of Brugada Syndrome is made when a type 1 pattern is present on the electrocardiogram (ECG), either spontaneously or after administration of a sodium channel blocker. For pathofysiological understanding, the investigators will analyse echocardiography images before and during the administration of Ajmaline. Comparing echocardiographies before and during negative Ajmaline test, will allow the investigators to indentify the effect of Ajmaline administration on cardiac function. The comparison between images of negative and positive Ajmaline tests will expose differences related to the occurence of a type 1 ECG.

Interventions

DRUGAjmaline test

Administration of Ajmaline

Sponsors

Universitair Ziekenhuis Brussel
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

* \>17 years old * clinical indication for Ajmaline test

Exclusion criteria

* History of right ventricular outflow tract ablation

Design outcomes

Primary

MeasureTime frameDescription
Speckle tracking strain measurement1 day at the time of enrollmentCardiac function assessed by speckle tracking peak strain and peak strain dispersion

Countries

Belgium

Contacts

Primary ContactEsther Scheirlynck, MD
esther.scheirlynck@uzbrussel.be+3228012461
Backup ContactIngrid Lemoine
ingrid.lemoine@uzbrussel.be

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026