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Vivistim Registry for Paired VNS Therapy (GRASP)

RecruitingObservational study

Who can join

Ages 22 and older · All sexes

Full eligibility criteria
Inclusion Criteria:

* Patients implanted with the Vivistim System for upper limb deficits associated with an ischemic stroke

Exclusion Criteria:

* Not eligible for surgery

About the 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.

What is being tested

Sponsor: MicroTransponder Inc. · Participants: 1,000 · Started: Mar 15, 2023

Contact the study team

Official record on ClinicalTrials.gov — NCT05301140

Locations in the U.S.

FloridaAdvent Health Orlando, Orlando
IllinoisAlexian Brothers Health System, Elk Grove Village
Endeavor Health, Evanston
KansasUniversity of Kansas Medical Center, Kansas City
KentuckyUniversity of Kentucky Research Foundation, Lexington
New JerseyOverlook Medical Center-Atlantic Health, Morristown
New YorkAlbany Medical College, Albany
Mt. Sinai, New York
Burke Rehabilitation Hospital, White Plains
PennsylvaniaJefferson Health - Lehigh Valley Health Network, Allentown
Thomas Jefferson, Philadelphia
Allegheny General Hospital, Pittsburgh
Allied Services Institute of Rehabilitation Medicine, Scranton
TexasPhysical Medicine and Neurotoxin Institute, Austin
St David's Medical Center, Austin

Conditions

From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.