Clinical Trials Logo

Clinical Trial Summary

An atrial septal defect (ASD) is a hole in the heart that can lead to heart failure. Depending on the size and severity of the ASD, They can be treated during a heart catheterization with a special device that can permanently seal the ASD, but knowing the exact size and severity of the ASD is crucial. Newer MRI techniques may provide a better way at diagnosing the size and severity of an ASD. We compared MRI to other standard clinical ways for evaluating an ASD.


Clinical Trial Description

Background: Atrial septal defect (ASD) flow can be measured indirectly by velocity-encoded cardiovascular magnetic resonance (veCMR) of the pulmonary artery and aorta (Qp/Qs). Imaging the secundum ASD en face could potentially enable direct flow measurement and, additionally, provide valuable information regarding ASD size, shape, location, and proximity to other structures. Methods: Patients referred for possible transcatheter ASD closure underwent a comprehensive standard evaluation including transesophageal and/or intracardiac echocardiography (ICE), and invasive oximetry. CMR was performed in parallel and included direct en face veCMR after an optimal double-oblique imaging plane was determined accounting for ASD flow direction and cardiac-cycle interatrial septal motion. We hypothesized that En face veCMR using an optimized imaging plane can accurately determine ASD flow, size, and morphology, and that it would provide information incremental to comprehensive standard evaluation. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT00498446
Study type Observational
Source Duke University
Contact
Status Completed
Phase
Start date July 2002
Completion date July 2004

See also
  Status Clinical Trial Phase
Completed NCT01120964 - Intravenous L-Citrulline to Treat Children Undergoing Heart Bypass Surgery : Revised Protocol Phase 1/Phase 2
Active, not recruiting NCT04950192 - Philips Intracardiac Echocardiography (ICE) Clinical Registry
Completed NCT02621528 - Lifetech CeraFlex™ Post-Market Surveillance Study N/A
Recruiting NCT04291898 - Comparison of Devices for Atrial Septal Defects Closure: A Pilot Study N/A
Terminated NCT01773252 - Right to Left Cardiac Shunt Detection Phase 3
Not yet recruiting NCT06344494 - Cardiac Interventional ICE Imaging Trial N/A
Not yet recruiting NCT05887700 - Lifetech CeraFlex™ ASD Closure System Post-Market Clinical Follow-Up
Recruiting NCT06298344 - The Role of Thiamine After Transcatheter Closure in Children With Left-to-Right Shunt Congenital Heart Disease Early Phase 1
Recruiting NCT06431178 - General Anesthesia Versus Sedation By Dexmedetomidine and Ketamine With Local Infiltration for Percutaneous Transcatheter Closure of Atrial Septal Defect in Pediatric Patients N/A
Active, not recruiting NCT04105595 - Post Market Registry of the CBSO
Recruiting NCT05688670 - Regional Anesthesia Following Pediatric Cardiac Surgery Phase 4
Active, not recruiting NCT02739087 - Radiation-Free Heart Catheterization Using MRI N/A
Recruiting NCT02097758 - Efficacy of Three Dimensional Transesophageal Echocardiography for Percutaneous Device Closure in Atrial Septal Defect N/A
Completed NCT02985684 - Safety and Efficacy Study of Transcatheter Closure of Ostium Secundum ASDs N/A
Completed NCT06139679 - Improvement In Left Ventricular Diameter After Closure Of ASD With Fenestrated Patch: A Cross-sectional Study
Recruiting NCT05540769 - Holter and ECG Changes After Transcatheter Closure Of ASD In Children N/A
Recruiting NCT04096924 - A Prospective Randomized Multicenter Trial of the Guidewire for Echo-guided Interventions N/A
Enrolling by invitation NCT02766569 - International Registry for ASD Closure by Using the Occlutech®Flex II Device in More Than 2000 Patients N/A
Completed NCT02957201 - The Effect on EPCs by Successful Cardiac Occlusion Device Implantation N/A
Recruiting NCT02453451 - The Effect of the Hole in the Cardiac Septum Developed by the MitraClip Procedure on the Blood Flow Mechanics N/A