North Shore University Hospital
Manhasset, New York, 11030, United States
Location status: Recruiting
NCT Number: NCT04758624
The purpose of this study is to elucidate the structural connectivity of the dentato-rubro-thalamic tract (DRTt) and to detect functional network changes due to DRTt stimulation
Interested in participating?
Request Info18 year–85 year
All sexes
Interventional
Not applicable
Manhasset, New York, 11030, United States
Location status: Recruiting
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Medtronic Activa device will be implanted and administered clinically, except as part of the trial after 24 months of DBS being on it will be turned off for 3 days and will be turned back on.
Time frame: Baseline before DBS implant
Time frame: 24 months after start of DBS
Time frame: Baseline before DBS implant
Time frame: 24 months after start of DBS
Time frame: Baseline before DBS implant
Time frame: 24 months after start of DBS
Time frame: Baseline before DBS implant
Time frame: 24 months after start of DBS
Time frame: Baseline before DBS implant
Time frame: 24 months after start of DBS
Time frame: Baseline before DBS is turned off
Time frame: 72 hours after DBS is turned off
Time frame: Baseline before DBS implant
10 items are measured-each is scored from 0-4,higher number indicating more tremor
Time frame: 24 months after start of DBS
10 items are measured-each is scored from 0-4,higher number indicating more tremor
Time frame: Baseline before DBS is turned off
10 items are measured-each is scored from 0-4,higher number indicating more tremor
Time frame: 72 hours after DBS is turned off
10 items are measured-each is scored from 0-4,higher number indicating more tremor
Time frame: During DBS placement surgery before active DBS
10 items are measured-each is scored from 0-4,higher number indicating more tremor
Time frame: During DBS placement surgery during active DBS
10 items are measured-each is scored from 0-4,higher number indicating more tremor
Time frame: During DBS placement surgery before active DBS
Time frame: During DBS placement surgery during active DBS
Time frame: Baseline before DBS implant
It has eight categories with accumulative score ranging from 0 (no ataxia) to 40 (most severe ataxia).
Time frame: 24 months after start of DBS
It has eight categories with accumulative score ranging from 0 (no ataxia) to 40 (most severe ataxia).
Time frame: Baseline before DBS is turned off
It has eight categories with accumulative score ranging from 0 (no ataxia) to 40 (most severe ataxia).
Time frame: 72 hours after DBS is turned off
It has eight categories with accumulative score ranging from 0 (no ataxia) to 40 (most severe ataxia).
Time frame: Baseline before DBS is turned off
Time frame: 72 hours after DBS is turned off
Interested in participating?
Request InfoNorthwell Health
Other
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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