Investigation of hemodynamic changes during balloon occlusion test for percutaneous atrial septal defect closure

Investigation of hemodynamic changes during balloon occlusion test for percutaneous atrial septal defect closure - The balloon occlusion during ASD closure

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

JPRN

Registry ID

JPRN-UMIN000023413

Enrollment

100

Registered

2016-07-31

Start date

2012-07-01

Completion date

Unknown

Last updated

2026-06-29

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

Conditions

Atrial septal defect

Interventions

None listed

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: prospective observational study Significant left-to-right shunt, right ventricular (RV) volume overload, and/or clinical symptoms of heart failure or paradoxical embolism Atomically feasible for percutaneous ASD closure

Exclusion criteria

Exclusion criteria: Eisenmenger physiology

Design outcomes

Primary

Measure	Time frame
Primary endpoint is the composite events including cardiac death, heart failure during hospitalization, heart failure after discharge , adjunctive diuretics, de novo palpitation and stroke after ASD closure.	—

Secondary

Measure	Time frame
Secondary endpoints New York Heart Assoission classification	—

Countries

Japan

Contacts

Public ContactHiroyuki Yamamoto

Department of Internal Medicine, Kobe University Graduate School of Medicine Division of Cardiovascular Medicine

y0493589m@hotmail.co.jp078-382-5846

Outcome results