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Clinical Research Directory

Browse clinical research sites, groups, and studies.

8 clinical studies listed.

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Brainstem Stroke

Tundra lists 8 Brainstem Stroke clinical trials. Each listing includes eligibility criteria, study locations, and direct links to research sites in the Tundra directory.

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RECRUITING

NCT07205263

RAINBOW-ICH Trial of AI Guided Minimally Invasive Neurosurgery for ICH

Intracerebral hemorrhage (ICH) is one of the most devastating forms of stroke, with high rates of death and disability worldwide. Despite advances in medical and surgical care, effective therapeutic options remain limited. To address this gap, the RAINBOW-ICH trial has been designed as a nationwide, multicenter, randomized umbrella trial evaluating the efficacy and safety of AI-assisted, robotic-guided minimally invasive neurosurgery compared with conventional strategies across major ICH subtypes. Under a single master protocol, RAINBOW-ICH incorporates multiple parallel randomized controlled substudies, each targeting a distinct ICH population-large basal ganglia hemorrhage, moderate basal ganglia hemorrhage, intraventricular hemorrhage, and brainstem hemorrhage. This umbrella design allows efficient use of resources while generating high-quality evidence tailored to the specific needs of different ICH subgroups, thereby supporting a more patient-centered approach to care.

Gender: All

Ages: 18 Years - Any

Updated: 2026-01-08

1 state

Basal Ganglia Hemorrhage
Intraventricular Hemorrhage
Brainstem Stroke
+1
RECRUITING

NCT06511934

Feasibility of the BrainGate2 Neural Interface System in Persons With Tetraplegia (BG-Tablet-01)

People with brainstem stroke, advanced amyotrophic lateral sclerosis (ALS, also known as Lou Gehrig's disease), or other disorders can become unable to move or speak despite being awake and alert. In this project, the investigators seek to further translate knowledge about interpreting brain signals related to movement, and to further develop an intracortical brain-computer interface (iBCI) that could restore rapid and intuitive use of communication apps on tablet computers by people with paralysis.

Gender: All

Ages: 18 Years - 80 Years

Updated: 2025-12-01

1 state

Brainstem Stroke
ALS
Tetraplegia
+2
RECRUITING

NCT01894802

Cortical Recording and Stimulating Array Brain-Machine Interface

The purpose of this research study is to demonstrate the safety and efficacy of using two CRS Arrays (microelectrodes) for long-term recording of brain motor cortex activity and microstimulation of brain sensory cortex.

Gender: All

Ages: 22 Years - 70 Years

Updated: 2025-10-20

2 states

Tetraplegia
Spinal Cord Injury
Brainstem Stroke
+2
RECRUITING

NCT06207591

Investigation on the Cortical Communication System

The goal of this clinical trial is to demonstrate communication through a brain implant in people in locked-in state, i.e. people with severe paralysis and communication problems. The main questions it aims to answer are efficient and stable control of Brain-Computer interface (BCI) functions for communication with attempted hand movements and operation of a keyword-based speech BCI. Participants will be implanted with four electrode grids, with in total 128 electrodes, on the surface of the brain and a connector on the skull. Participation includes visits of researchers for recording and training at home, 2-3 times per week for one year. Extension of participation after one year is possible. If successful, the participant will be able to use the BCI at home independently, without the presence of a researcher.

Gender: All

Ages: 18 Years - 70 Years

Updated: 2025-10-03

Locked-in Syndrome
Neuromuscular Diseases
Brainstem Stroke
+1
RECRUITING

NCT03567213

Investigation on the Cortical Communication (CortiCom) System

The CortiCom system consists of 510(k)-cleared components: platinum PMT subdural cortical electrode grids, a Blackrock Microsystems patient pedestal, and an external NeuroPort Neural Signal Processor. Up to two grids will be implanted in the brain, for a total channel count of up to 128 channels, for six months. In each participant, the grid(s) will be implanted over areas of cortex that encode speech and upper extremity movement.

Gender: All

Ages: 22 Years - 70 Years

Updated: 2025-07-25

1 state

Tetraplegia
Locked-in Syndrome
Brainstem Stroke
+1
NOT YET RECRUITING

NCT06944834

A Study on the Safety and Functionality of the Implantable Wireless Brain-Computer Interfaces for Motor Rehabilitation

The objective of this study is to evaluate the safety and efficacy of minimally invasive, wireless brain-machine interface system (WRS) in patients with paralysis (resulting from spinal cord injuries, brainstem strokes, amyotrophic lateral sclerosis, or other motor neuron diseases causing complete or incomplete quadriplegia) or bilateral upper limb amputations. By leveraging brain-machine interface alternative technology, participants can use brain signals to control external devices (such as moving cursors, wheelchairs, robotic arms, WeChat Mini Programs, and other physical assistive devices), thereby improving their motor function and quality of life.

Gender: All

Ages: 18 Years - 65 Years

Updated: 2025-04-25

1 state

Quadriplegia
Amputations
Spinal Cord Injuries (SCI)
+1
RECRUITING

NCT06829212

Research on Wireless Brain Implant System for General Control of External Devices

The clinical trial aims to evaluate the safety and efficacy of the minimally invasive, wireless brain-machine interface system (WRS) in enabling general brain control of external devices, such as a cursor and other assistive technologies, for paralyzed and amputee patients. WRS integrates a high-throughput, ultra-flexible neural electrode with an extremely small cross-sectional size-approximately one-hundredth the diameter of a human hair. Moreover, the implantable component is fully embedded within the body, leaving no visible external traces.

Gender: All

Ages: 18 Years - 80 Years

Updated: 2025-03-13

1 state

Complete or Incomplete Paraplegia/quadriplegia
Spinal Cord Injury
Brainstem Stroke
+2
RECRUITING

NCT06091332

Hemorrhagic Brainstem Cavernous Malformations Treatment With Sirolimus: aSingle Centre, Randomized, Placebo-controlled Pilot Trial

The aim of this pilot phase trial is to assess the safety and tolerability, and estimate the efficacy of sirolimus in reducing the incidence of ICH during high-risk periods for rebleeding, compared to placebo. This pilot trial will inform the design of a future definitive clinical trial on sirolimus treatment for CCM.

Gender: All

Ages: 18 Years - 65 Years

Updated: 2024-12-20

1 state

Cavernous Malformations
Intracerebral Hemorrhage
Brainstem Stroke