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BIO|CONCEPT.Amvia, First in Human Study for the Amvia/Solvia Pacemaker Family
The goal of this exploratory study is to test the preliminary safety and product performance of the new Amvia/Solvia pacemaker family in subjects that require a pacemaker or cardiac resynchronization therapy pacemaker (CRT-P) implantation. The study will be conducted at sites in Australia and New Zealand. It is planned to include 50 subjects in the study. Participants will visit sites at enrollment in the study, at implantation, pre-hospital discharge, 1- 3- and 12-month follow-up visits. At the visits the device will be interrogated and standard device measurements including those related to special features will be performed to assess the functionality of the device. Programming of the pacemakers will be done according to the participant´s therapeutical needs.
Age
18 - No limit years
Sex
ALL
Healthy Volunteers
No
John Hunter Hospital
New Lambton Heights, New South Wales, Australia
Advara Heart Care Wesley
Auchenflower, Queensland, Australia
Gold Coast University Hospital
Southport, Queensland, Australia
Royal Hobart Hospital
Hobart, Tasmania, Australia
Peninsula Heart Centre
Frankston, Victoria, Australia
The Alfred Hospital
Melbourne, Victoria, Australia
Christchurch Hospital
Christchurch, New Zealand
Start Date
November 23, 2022
Primary Completion Date
June 11, 2024
Completion Date
June 11, 2024
Last Updated
July 24, 2025
52
ACTUAL participants
Amvia Sky pacemaker or CRT-P device
DEVICE
Lead Sponsor
Biotronik Australia Pty Ltd.
Collaborators
NCT07484009
NCT07191730
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
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