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NCT06761807

Electrocardiographic and Electrophysiologic Changes After Percutaneous Closure of Atrial Septal Defect

Not yet recruiting NA Last updated 7 January 2025
What this trial tests

NA trial testing Electrophysiology study of heart in ASD in 65 participants. Not yet recruiting.

Timeline
20 January 2025
Primary endpoint
2 November 2026
2 November 2027

Quick facts

Lead sponsorAssiut University
PhaseNA
StatusNot yet recruiting
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposediagnostic
Enrollment65
Start date20 January 2025
Primary completion2 November 2026
Estimated completion2 November 2027

Drugs / interventions tested

Conditions studied

Sponsor

Assiut University

Who can join

18 and older, any sex, with ASD or Brady Arrythmia. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Primary outcomes : Determining the incidence of SAN and AVN dysfunction before and after percutaneous ASD closure Comparing ECG and EP parameters of SAN and AVN before and after percutaneous ASD closure Secondary outcomes : Assessing clinical, echocardiographic and procedural risk factors affecting the AVN function after ASD closure device implantation Determining the incidence of supraventricular arrhythmia inducibility before and after percutaneous ASD closure

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for ASD

Currently open trials in the same condition.

Other Assiut University trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06761807.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing