Description Module
The Description Module contains narrative descriptions of the clinical trial, including a brief summary and detailed description. These descriptions provide important information about the study's purpose, methodology, and key details in language accessible to both researchers and the general public.
Description Module path is as follows:
Study -> Protocol Section -> Description Module
Description Module
Ignite Creation Date:
2025-12-24 @ 5:08 PM
Ignite Modification Date:
2025-12-24 @ 5:08 PM
NCT ID:
NCT05329350
Brief Summary:
The Occlutech® mVSD is indicated for percutaneous, transcatheter muscular ventricular septal defect closure device designed for the occlusion of hemodynamically 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.
Detailed Description:
This is a multicenter, International, follow-up registry to monitor the efficacy and safety of the Occlutech® mVSD in patients with muscular ventricular septal defects.
* Efficacy and safety of implanted device(s) will be assessed by vital signs, laboratory test, ECGs, and echocardiography on Day 1 (within 36 hrs. post procedure), Day 30, day 60, 6 months and 1 year after the implantation.
* Patients will be treated according to the instruction-for-use of the device and according to clinical routine
* Patients will be screened to determine eligibility for the registry based on inclusion/exclusion criteria, through their medical history, demographics, vital signs, clinical laboratory tests, performance of a 12 lead electrocardiogram (ECG) and echocardiography data.
* Procedures will be performed at sites having appropriate laboratory support and adequately trained imaging personnel. Procedure will be performed by physicians with experience in a wide range of interventional cardiology and structural heart disease, including transseptal puncture, anterograde, retrograde or transapical device delivery approaches.
Registry will be open for the next two years or when up to 100 patients are enrolled (whatever comes first)
The primary efficacy endpoints will include data obtained 1 year after mVSD closure procedure for successful implantation of the device with a proper closure of the mVSD (defined as Reduction in muscular ventricular septal regurgitation of ≥ one grade as assessed by echocardiography pre vs post implantation) and/or reduction in the number of hemolysis related transfusions.
The primary safety endpoint is defined as absence of Serious Adverse Events (SAEs) 1 years after mVSD closure procedure.
Study:
NCT05329350
Study Brief:
Protocol Section:
NCT05329350