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Study identifier: NCT05329350 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Follow-up Study to Monitor the Efficacy and Safety of the Occlutech® mVSD Cases

Condition: Muscular Ventricular Septal Defect  ·  Sponsor: Occlutech International AB

PhaseN/A
Planned participants50
Who can joinAll sexes, 3 Months to 80 Years
Healthy volunteersNo

About this study

The Occlutech® mVSD is indicated for percutaneous occlusion of hemodynamically or clinically significant muscular ventricular septal defects. The objectives of the study are: * To confirm the efficacy of Occlutech mVSD in patients requiring transcatheter occlusion (closure) of muscular ventricular septal defects. * To confirm the safety of Occlutech mVSD in patients requiring transcatheter occlusion (closure) of muscular ventricular septal defects.

This description comes directly from the study's public registry record.

Talk to the study team

Ahmed Della  ·  +49 151 14139961  ·  ahmed.dellaa@occlutech.com

Always discuss trial participation with your own doctor first.

Locations (5)

Children's Health IrelandDublin, IrelandNot Yet Recruiting
İzmir Şehir HastanesiIzmir, Bayraklı, Turkey (Türkiye)Not Yet Recruiting
Eskişehir Osmangazi Üniversite HastanesiEskişehir, Odunpazarı, Turkey (Türkiye)Not Yet Recruiting
Dicle Üniversitesi Tıp Fakültesi HastanesiDiyarbakır, Sur, Turkey (Türkiye)Not Yet Recruiting
Gaziantep Unıversıty HospitalGaziantep, Şehitkamil, Turkey (Türkiye)Recruiting

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Source record: clinicaltrials.gov/study/NCT05329350