About this trial

An study evaluating the long-term safety of all patients previously treated with NVDX3.

Eligibility criteria

Qualifiers

Patient being implanted with NVDX3.

Previously participated to one of the NVDX3 core clinical trials.

Patient accepts to comply to a yearly follow-up safety visit for 10 additional years

Patient has understood and accepted to participate in the long-term follow-up study by signing the informed consent.

Disqualifiers

None

Trial design

Treatments tested in this trial

  • NVDX3

Treatment groups

15 Participants
are divided into 1 treatment group

Locations

1
Centre Hospitalier de Luxembourg1210, Luxembourg Luxembourg

Sponsors and collaborators

Novadip Biosciences

Lead sponsor

PrimeVigilance

Collaborator

Data Investigation Company Europe (DICE)

Collaborator