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Septal Defect
Clinical trial pipeline · Data from ClinicalTrials.gov
See which Septal Defect trials may be worth asking aboutClinical trial pipeline · Data from ClinicalTrials.gov
See which Septal Defect trials may be worth asking aboutNorth America
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Trials may have sites in multiple countries. Filtering shows any trial with at least one site in the selected country.
The purpose of this study is to compile real-world data on patient outcomes and evaluate the procedural success and performance of the CeraFlex™ PFO Closure Sys…
The objective of this post-market registry is to assess the clinical use of the Lifetech CeraFlex™ Closure System in a real-world and on-label fashion.
This study will assess the safety and effectiveness of GORE® CARDIOFORM Septal Occluder in a post approval setting and evaluate the quality of operator educatio…
Ischemic stroke represents a major public health issue, leading to significant disabilities and deaths worldwide. When no clear cause for stroke is found follow…
The Abbott Structural Heart (SH) Registry is being conducted to confirm the safety and performance of Abbott's SH devices in a post-market, real-world setting.…
The goal of this observational study is to develop and validate a multimodal artificial intelligence prediction model for treatment-related complications in chi…
The goal of this observational study is to develop and test a AI-based prediction model for children with perimembranous ventricular septal defect, also called…
In this study, the investigators aim to compare the pressure gradient obtained by transesophageal echocardiography across the restrictive peri membranous VSD wi…
Multi-center, prospective, randomized, placebo- and sham-controlled study to evaluate the GORE® CARDIOFORM Septal Occluder for migraine headache relief