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Study identifier: NCT05301140 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Vivistim Registry for Paired VNS Therapy (GRASP)

Condition: Upper Extremity Problem  ·  Sponsor: MicroTransponder Inc.

PhaseN/A
Planned participants1000
Who can joinAll sexes, 22 Years to no upper limit
Healthy volunteersNo

About this study

The purpose of the Vivistim Registry for Paired VNS Therapy (GRASP) is to gather real-world information on patients with arm and hand deficits post-stroke who are considering Vivistim System treatment. Before and after Vivistim System implant, patient data will be collected and reported throughout the therapy process. Physicians or sites will receive appropriate remuneration for the effort and cost involved in collecting and transmitting this data to MicroTransponder Inc.

This description comes directly from the study's public registry record.

Talk to the study team

Brent Tarver, BSEE  ·  8556289375  ·  brent.tarver@mobia.com

Diana Hansen  ·  8556289375  ·  diana.hansen@mobia.com

Always discuss trial participation with your own doctor first.

Locations (15)

Advent Health OrlandoOrlando, Florida, United StatesRecruiting
Alexian Brothers Health SystemElk Grove Village, Illinois, United StatesRecruiting
Endeavor HealthEvanston, Illinois, United StatesRecruiting
University of Kansas Medical CenterKansas City, Kansas, United StatesRecruiting
University of Kentucky Research FoundationLexington, Kentucky, United StatesRecruiting
Overlook Medical Center-Atlantic HealthMorristown, New Jersey, United StatesRecruiting
Albany Medical CollegeAlbany, New York, United StatesRecruiting
Mt. SinaiNew York, New York, United StatesRecruiting
Burke Rehabilitation HospitalWhite Plains, New York, United StatesRecruiting
Jefferson Health - Lehigh Valley Health NetworkAllentown, Pennsylvania, United StatesRecruiting
Thomas JeffersonPhiladelphia, Pennsylvania, United StatesRecruiting
Allegheny General HospitalPittsburgh, Pennsylvania, United StatesRecruiting

+ 3 more locations — full list on the registry record.

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Source record: clinicaltrials.gov/study/NCT05301140