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Authors
Fontaine, Denys
Leplus, Aurélie
Donnet, Anne
Darmon, Nelly
Balossier, Anne
Giordana, Bruno
Simonet, Benoit
Isan, Petru
Regis, Jean
Lanteri-Minet, Michel
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Funding
Funding for this research was provided by:
Centre Hospitalier Universitaire de Nice (16-AOIP-01, 16-AOIP-01, 16-AOIP-01)
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Article History
Received: 1 January 2025
Accepted: 28 January 2025
First Online: 17 February 2025
Declarations
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: The study was approved by a Ethical Medical Committee (“Comité de Protection de Personnes Sud Méditerranée”, ID-IRB 2017-A00032-51) and registered (clinicaltrials.gov NCT03399942). All the patients signed an informed consent before inclusion. Safety data were supervised by an independent Data Monitoring Committee.
: This academic study has been sponsored and funded by the CHU de Nice (grant number: 16-AOIP-01). The hardware (leads and generators) was provided free of charge by Abbott which was not involved in the design and analysis of the study. DF is consultant for Medtronic, Abbott, and Boston Scientific, companies that manufacture and commercialize DBS devices, and received research grant from Medtronic and Abbott. MLM is consultant for Medtronic and received research grant from Medtronic. AL received speaker fees from Boston Scientific. AB has received consultant fees from Medtronic. Other authors declare no conflict of interest related to the study.
