Clinical Trials for Hemorrhagic Stroke

Currently registered clinical trials for Hemorrhagic Stroke from ClinicalTrials.gov. 26 recruiting, 50 total studies.

This content is for informational purposes only. Always consult a healthcare professional.

Source: ClinicalTrials.gov — U.S. National Library of Medicine — A database of privately and publicly funded clinical studies conducted around the world (U.S. National Library of Medicine, public domain).

This page lists clinical trials related to Hemorrhagic Stroke from the ClinicalTrials.gov database.

Trial Summary

  • Total studies: 50
  • Recruiting: 26
  • Active, not recruiting: 3
  • Completed: 8
  • Other: 13

Results are refreshed periodically and may not reflect the most current information available from ClinicalTrials.gov.

Recruiting Trials

NCT04078373 — Urinary Disorders in Subacute Patients After Stroke

StatusRecruiting
PhaseN/A
SponsorUniversity Rehabilitation Institute, Republic of Slovenia
Enrollment250
Study TypeOBSERVATIONAL
ConditionsStroke, Ischemic; Stroke Hemorrhagic; Urinary Incontinence
Interventions;

This observational study will address urinary disorders in subacute stroke patients. Patients without and with urinary disorders will be compared, and treatment outcome will be assessed among the latter.

NCT04975646 — Goal Attainment Scaling in Upper Limb Spasticity Treatment

StatusRecruiting
PhaseN/A
SponsorUniversity Rehabilitation Institute, Republic of Slovenia
Enrollment70
Study TypeINTERVENTIONAL
ConditionsIschemic Stroke; Hemorrhagic Stroke
Interventions

Patients after stroke with upper limb spasticity treated with botulinum toxin-A (BTX-A) will be included in this two-part study. In the first part, goal attainment scaling and comprehensive assessment of motor functioning will be performed before BTX-A application and after two weeks. In the second part, the patients will be randomised into a test group performing prescribed regular exercise fo…

NCT05085210 — Improving Visual Field Deficits With Noninvasive Brain Stimulation

StatusRecruiting
PhaseN/A
SponsorBeth Israel Deaconess Medical Center
Enrollment24
Study TypeINTERVENTIONAL
ConditionsVisual Field Defect, Peripheral; Stroke; Visual Impairment; Hemianopsia; Quadrantanopia
Interventions; ;

This is a randomized, pilot interventional study in participants with visual field deficit (VFD) caused by cortical lesion. Damage to the primary visual cortex (V1) causes a contra-lesional, homonymous loss of conscious vision termed hemianopsia, the loss of one half of the visual field. The goal of this project is to elaborate and refine a rehabilitation protocol for VFD participants. It is hy…

NCT05113043 — Correlation Between Intestinal Microecology Imbalance and Stroke in Young Adults

StatusRecruiting
PhaseN/A
SponsorShanghai 6th People’s Hospital
Enrollment60
Study TypeOBSERVATIONAL
ConditionsIschemic Stroke; Hemorrhagic Stroke

The relationship between the intestinal microecology and stroke has become a research hotspot in neurology field today. Maintaining the balance of the intestinal microbiota are expected to bring new breakthroughs for prevention and treatment of stroke. In recent years, stroke in young adults has an increasing incidence and a considerable socioeconomic impact because of high disability rate and …

NCT05140148 — Promoting Recovery After STroke With Amantadine

StatusRecruiting
PhasePhase 2
SponsorUniversity of Pennsylvania
Enrollment60
Study TypeINTERVENTIONAL
ConditionsStroke, Ischemic; Stroke Hemorrhagic
Interventions;

The investigators aim to examine whether amantadine can help patients recover from stroke. This will be a blinded randomized clinical trial (RCT). Patients will be randomized post-ischemic or hemorrhagic stroke either to the placebo arm or amantadine arm. Patients will be on study drug or placebo for 1 month but will be enrolled for 3 months total. At various time points patients will be examin…

NCT06001736 — Utility of CC7 Transfer in Stroke Subtypes

StatusRecruiting
PhaseN/A
SponsorDartmouth-Hitchcock Medical Center
Enrollment95
Study TypeINTERVENTIONAL
ConditionsStroke, Ischemic; Stroke Hemorrhagic; Spastic Hemiparesis
Interventions

The purpose of this study is to evaluate the limb functional improvement after contralateral C7 root transfer in stroke patients.

NCT05300997 — Translational Immunodiagnostics in Stroke (TrImS)

StatusRecruiting
PhaseN/A
SponsorThe University of Hong Kong
Enrollment650
Study TypeOBSERVATIONAL
ConditionsAcute Ischemic Stroke; Haemorrhagic Stroke; Transient Ischemic Attacks; Cardioembolic Stroke; Large-Artery Atherosclerosis (Embolus/Thrombosis)
Interventions

In adult patients presenting to emergency departments within 24 hours of symptom onset with suspected acute stroke, we aim:

  1. to identify early brain- and pathology-specific circulating, whole blood, plasma and serum panorOmic biomarkers that enable early acute stroke detection, diagnosis, dynamics, differentiation, monitoring, prediction and prognosis.
  2. to identify early brain- and patholo…

NCT05393492 — Regulating Emotions and Behaviors After Brain Injury

StatusRecruiting
PhaseN/A
SponsorUniversity Hospital, Strasbourg, France
Enrollment77
Study TypeINTERVENTIONAL
ConditionsAcquired Brain Injury; Stroke/ Cerebrovascular Accident (Ischemic or Hemorrhagic); Brain Tumor (After Recovery); Encephalitis; Cerebral Anoxia
Interventions

After acquired brain injury (ABI), persons can experience emotional and behavioral difficulties, that can be painful both for the person and his/her family. This clinical study aims at measuring the effectiveness of a third wave cognitive behavioral therapy called “dialectical behavior therapy” (DBT). DBT aims at teaching persons emotion regulation skills, interpersonal effectiveness skills, mi…

NCT04427241 — Efficacy and Safety of Cerebrolysin on Prolonged Disorders of Consciousness

StatusRecruiting
PhasePhase 4
SponsorKonkuk University Medical Center
Enrollment12
Study TypeINTERVENTIONAL
ConditionsDisorder of Consciousness; Hemorrhagic Stroke
Interventions;

Object: To determine the effect of cerebrolysin on prolonged disorders of consciousness caused by hemorrhagic stroke.

Participants: patients with prolonged disorders of consciousness due to severe traumatic brain injury

Intervention: 30 ml cerebrolysin + 70 ml normal saline, days 4-17, once/day, intravenously or 100 ml normal saline, days 4-17, once/day, IV

Comparison: cerebrolysin group ver…

NCT07614074 — Recovery Trajectory for Coma and Disorders of Consciousness

StatusRecruiting
PhaseN/A
SponsorUniversity of California, San Francisco
Enrollment2000
Study TypeOBSERVATIONAL
ConditionsComa; Disorders of Consciousness; Cardiac Arrest (CA); Traumatic Brain Injuries; Ischemic Stroke

This study aims to better understand recovery after coma caused by serious neurologic illness or injury. Patients who are unconscious (in a coma or disorder of consciousness) due to conditions such as stroke, cardiac arrest, traumatic brain injury, seizures, brain infection, or other neurologic emergencies may be enrolled during their hospitalization.

The purpose of this observational research…

NCT05884762 — earlY Upper Limb Rehabilitation WIth EEG-Neurofeedback After Stroke

StatusRecruiting
PhaseN/A
SponsorRennes University Hospital
Enrollment40
Study TypeINTERVENTIONAL
ConditionsStroke; Stroke Hemorrhagic; Stroke, Ischemic; Stroke Rehabilitation; Brain Infarction
Interventions;

The aim of this study is to evaluate the effect of early rehabilitation treatment by electroencephalographic neurofeedback on upper limb motor function after stroke.

Researchers will compare :

Interventional group: electroencephalographic neurofeedback + traditional reference rehabilitation programme Control group: SHAM electroencephalographic neurofeedback + traditional reference rehabilitat…

NCT06127602 — The REACTplusNMES Trial: A Double-blinded RCT

StatusRecruiting
PhaseN/A
SponsorUniversity of Illinois at Chicago
Enrollment46
Study TypeINTERVENTIONAL
ConditionsStroke, Ischemic; Stroke Hemorrhagic; Stroke, Cerebrovascular
Interventions;

The aim of this study is to compare the effectiveness of 6-weeks of reactive balance training (REACT) with and without neuromuscular electrical stimulation (NMES) to paretic lower limb muscles on biomechanical, clinical, neuromuscular and neuroplastic outcomes of reactive balance control. This project is a Phase-I study and incorporates a double-blinded, randomized controlled trial design.

Met…

NCT06308952 — Atorvastatin Pretreatment in Cerebrovascular Events (APICES) After Flow Diverter Implantation

StatusRecruiting
PhasePhase 4
SponsorDuan Chuanzhi
Enrollment354
Study TypeINTERVENTIONAL
ConditionsCerebrovascular Event; Stent Stenosis; Ischemic Stroke; Hemorrhagic Stroke; Stent Thrombosis
Interventions

APICES trial is an investigator-initiated, multicenter, multicenter, randomized, double-blind, placebo-controlled clinical trial that plans to enroll 396 patients with a 1-year follow-up, including a neurovascular imaging examination [digital subtraction angiography (DSA), CT angiography (CTA) or magnetic resonance angiography (MRA)] at 6 months after index treatment. It was designed in compl…

NCT06094478 — Hospital Implementation of a Stroke Protocol for Emergency Evaluation and Disposition

StatusRecruiting
PhaseN/A
SponsorUniversity of Chicago
Enrollment900
Study TypeINTERVENTIONAL
ConditionsStroke, Acute; Ischemic Stroke, Acute; Hemorrhagic Stroke
Interventions

Most stroke patients are initially evaluated at the closest hospital but some need to be transferred to a hospital that can provide more advanced care. The “Door-In-Door-Out” (DIDO) process at the first hospital can take time making transferred patients no longer able to get the advanced treatments. This study will help hospitals across the US “stand up” new ways to evaluate stroke patients, de…

NCT00682695 — Genetic and Environmental Risk Factors for Hemorrhagic Stroke

StatusRecruiting
PhaseN/A
SponsorState University of New York at Buffalo
Enrollment1000
Study TypeOBSERVATIONAL
ConditionsStroke

The purpose of this study is to find risk factors for hemorrhagic stroke.

NCT07227246 — Recombinant Factor VIIa (rFVIIa) for Hemorrhagic Stroke Trial - Part 2

StatusRecruiting
PhasePhase 3
SponsorJoseph Broderick, MD
Enrollment350
Study TypeINTERVENTIONAL
ConditionsIntracerebral Hemorrhage
Interventions;

The objective of the rFVIIa for Acute Hemorrhagic Stroke Administered at Earliest Time (FASTEST) Trial is to establish the first treatment for acute spontaneous intracerebral hemorrhage (ICH) within a time window and subgroup of patients that is most likely to benefit. The central hypothesis is that rFVIIa, administered within 120 minutes from stroke onset with an identified subgroup of patient…

NCT06870812 — Rapid Evacuation and Access of Cerebral Hemorrhage Trial

StatusRecruiting
PhaseN/A
SponsorEmory University
Enrollment600
Study TypeINTERVENTIONAL
ConditionsStroke Hemorrhagic
Interventions;

The main purpose of this study is to compare patients with a deep bleed in the brain undergoing surgery to patients receiving routine medical care. The standard treatment involves admission to the Intensive Care Unit (ICU) with close monitoring and blood pressure control. It also includes other medical (non-surgical) treatments to prevent more bleeding or another stroke. Sometimes, doctors will…

NCT07019493 — Young Stroke Service Deep Phenotyping: Exploring Recovery in Young Adult Survivors of Stroke

StatusRecruiting
PhaseN/A
SponsorThe Florey Institute of Neuroscience and Mental Health
Enrollment100
Study TypeOBSERVATIONAL
ConditionsStroke Patients; Stroke; Stroke; Sequelae; Young Adults
Interventions

The Investigators are running a small, early-phase research study across several hospitals in Melbourne, Australia. The study will involve up to 100 young adults between the ages of 18 and 55 who have had a stroke. The goal is to test how practical it is to carry out a detailed health assessment process-called “deep phenotyping”-with this group.

This process involves collecting a wide range of…

NCT07113067 — Accelerated rTMS vs. Sham for Stroke Apathy

StatusRecruiting
PhasePhase 1 / Phase 2
SponsorMedical University of South Carolina
Enrollment40
Study TypeINTERVENTIONAL
ConditionsApathy; Stroke; Stroke Sequelae; Stroke/Brain Attack; Stroke/ Cerebrovascular Accident (Ischemic or Hemorrhagic)
Interventions; ;

Apathy is a common set of symptoms seen in many people following a stroke. Apathy occurs when a person has lost motivation, becomes withdrawn, and stops doing things that used to be important to them. Apathy has a large negative impact on a person’s quality of life, and can also have a large impact the people who take care of them. There are currently no FDA-approved treatments to help with apa…

NCT07474935 — Targeting Real World Usage In Stroke Treatment

StatusRecruiting
PhaseN/A
SponsorPhenox GmbH
Enrollment5000
Study TypeOBSERVATIONAL
ConditionsSaccular and Fusiform Aneurysms; Pseudoaneurysm; Vascular Dissection; Perforation; Bifurcation Aneurysms
Interventions; ;

TRUST Registry is an observational, prospective, long-term, post-market surveillance registry of subjects treated with WallabyPhenox flow modulation devices, stent systems, bifurcation aneurysm implants including their HPC variants (Hydrophilic Polymer Coating) where applicable as well as coil systems, and other adjunctive medical devices.

The overarching purpose of this registry is to carry o…

NCT07237048 — Minocycline in Stroke Study at Maimonides

StatusRecruiting
PhasePhase 2 / Phase 3
SponsorJoyce Chen
Enrollment1164
Study TypeINTERVENTIONAL
ConditionsStroke; Ischemia Stroke; Hemorrhagic Strokes; Mortality; Morbidity
Interventions

The goal of this study is to determine if Minocycline, when added to standard care, can improve survival and functional outcomes in patients with moderate acute stroke (ischemic or hemorrhagic) aged 18 years and older.

The main questions it aims to answer are:

  1. Does Minocycline improve *National Institutes of Health Stroke Scale* (NIHSS) scores at hospital discharge and 90 days post-strok…

NCT07143019 — The Use of p48/64 MW HPC Flow Modulation Device in the Treatment of Wide-necked Intracranial Aneurysms

StatusRecruiting
PhaseN/A
Sponsorphenox Inc.
Enrollment214
Study TypeINTERVENTIONAL
ConditionsHemorrhagic Stroke; Aneurysm, Intracranial; Saccular Aneurysm; Fusiform Aneurysm; Brain Aneurysm
Interventions

To determine safety and effectiveness of the p48 MW HPC and p64 MW HPC Flow Modulation Device in the treatment of wide-necked intracranial aneurysms.

NCT07635498 — Virtual Stroke Units Versus Conventional Stroke Unit Care in Non-Thrombectomy-Candidate Patients.

StatusRecruiting
PhaseN/A
SponsorHospital Universitario Virgen Macarena
Enrollment726
Study TypeOBSERVATIONAL
ConditionsStroke; Stroke Hemorrhagic; Ischemic Stroke
Interventions;

Stroke is the leading cause of acquired disability in adults and a major cause of mortality worldwide; in Spain, Andalusia shows the highest stroke-related mortality rate. Comprehensive Stroke Units (SU) are the gold-standard organizational model for acute stroke care; however, only a fraction of patients have direct access to an SU, particularly those not eligible for mechanical thrombectomy w…

NCT07627399 — Effectiveness of Best Care Practices in Acute Stroke in Conventional Hospitalization (BEST CARE ICTUS_HC)

StatusRecruiting
PhaseN/A
SponsorUniversity of Malaga
Enrollment700
Study TypeINTERVENTIONAL
ConditionsStroke; Acute Stroke; Ischemic Stroke; Hemorrhagic Stroke; Cerebrovascular Disorders
Interventions

The goal of this clinical trial is to evaluate whether a multicomponent nurse-led intervention (BEST CARE ICTUS_HC) can reduce stroke-related complications and improve recovery in adults (18 years and older) hospitalized with an acute ischemic or hemorrhagic stroke in hospitals without specialized Stroke Units. The main questions it aims to answer are:

  1. Does the implementation of the progra…

NCT07631078 — kTMP-Enhanced Motor Rehabilitation for Chronic Stroke Recovery (KULMINATE) Pilot

StatusRecruiting
PhaseN/A
SponsorMagnetic Tides
Enrollment12
Study TypeINTERVENTIONAL
ConditionsStroke; Chronic Stroke Patients; Arm Weakness as a Consequence of Stroke
Interventions;

kTMP, kilohertz transcutaneous magnetic perturbations, is a low intensity transcranial magnetic stimulation technique that will be used in this study to promote arm/hand rehabilitation in patients who have been disabled by stroke.

NCT07649135 — Feasibility of a Remotely Delivered Step Count Intervention in Chronic Stroke

StatusRecruiting
PhaseN/A
SponsorUniversity of Minnesota
Enrollment24
Study TypeINTERVENTIONAL
ConditionsStroke; Ischemic Stroke; Hemorrhagic Stroke
Interventions

The goal of this study is to explore the feasibility of a new approach to rehabilitation that focuses on step count. Participants will complete 6 telephone or Zoom-based sessions with an occupational therapist over 6 weeks and use a step count tracker during that time. They will also complete questionnaires, assessments, surveys, and physical activity measurements during study weeks 0 (baseline…

Active, Not Recruiting

NCT03950076 — EdoxabaN foR IntraCranial Hemorrhage Survivors With Atrial Fibrillation (ENRICH-AF)

StatusActive, not recruiting
PhasePhase 4
SponsorPopulation Health Research Institute
Enrollment948
Study TypeINTERVENTIONAL
ConditionsIntracranial Hemorrhages; Atrial Fibrillation
Interventions;

To assess whether edoxaban (60/30 mg daily) compared to non-antithrombotic medical therapy (either no antithrombotic therapy or antiplatelet monotherapy) reduces the risk of stroke (composite of ischemic, hemorrhagic and unspecified stroke) or systemic embolism in high-risk atrial fibrillation (CHA2DS2-VASc ≥2) patients with previous intracranial hemorrhage.

NCT05089331 — ROSE-Longitudinal Assessment With Neuroimaging

StatusActive, not recruiting
PhaseN/A
SponsorState University of New York at Buffalo
Enrollment250
Study TypeOBSERVATIONAL
ConditionsIntracerebral Hemorrhage

The investigators will perform follow-up on 250 of 500 cases recruited into the ROSE study of cases with deep and lobar intracerebral hemorrhage to perform advanced neuroimaging at 12-24 months post stroke, and evaluations of motor and cognitive function at baseline, 6 months after baseline, and 12 months after baseline to determine predictors of recovery, progressive cognitive or functional im…

NCT05397106 — Post Market Clinical Follow-up of CODMAN CERTAS Programmable Valve

StatusActive, not recruiting
PhaseN/A
SponsorIntegra LifeSciences Corporation
Enrollment160
Study TypeOBSERVATIONAL
ConditionsHydrocephalus; Hydrocephalus in Children; NPH (Normal Pressure Hydrocephalus); IIH - Idiopathic Intracranial Hypertension; Brain Tumor
Interventions

Post-Market Clinical Follow-up Registry of Patients with CODMAN CERTAS Plus Programmable Valves.

Not Yet Recruiting

NCT07433972 — Changes in Hemodynamic Response Following Transcranial Electrical Stimulation in Sroke Individuals

StatusNot yet recruiting
PhaseN/A
SponsorMahidol University
Enrollment60
Study TypeINTERVENTIONAL
ConditionsHemorrhagic Stroke; Ischemic Stroke; Subacute Stroke; Chronic Stroke Survivors
Interventions; ;

The present study will use transcranial electrical stimulation (tES) which are transcranial direct current stimulation (tDCS) and transcranial alternating current stimulation (tACS) combined with conventional physical therapy and cognitive-motor dualt ask gait training in sub-acute (at least 2 weeks after stroke onset) to chronic stroke (within 5 years post-stroke) to investigate changes in bra…

NCT07511868 — Digital Application for Stroke Health

StatusNot yet recruiting
PhaseN/A
SponsorVASCage GmbH
Enrollment500
Study TypeINTERVENTIONAL
ConditionsHaemorrhagic Stroke; Ischaemic Stroke; Transient Ischemic Attack (TIA)
Interventions;

Stroke is a leading cause of death and long-term disability worldwide. Despite substantial advances in acute stroke care, there remains a lack of evidence-based digital solutions to support patients after hospital discharge. This study evaluates the effectiveness of a digital health application (StrokeApp) designed to support patients with ischemic or hemorrhagic stroke or transient ischemic at…

NCT07665827 — Efficacy and Safety of Antihypertensive Treatment With Mobile Stroke Units in Ultra-Early Intracerebral Hemorrhage

StatusNot yet recruiting
PhaseN/A
SponsorXuanwu Hospital, Beijing
Enrollment706
Study TypeINTERVENTIONAL
ConditionsNervous System Diseases; Cerebrovascular Disorders; Cardiovascular Diseases; Vascular Diseases; Hemorrhage
Interventions;

MSU-ICH is a prospective, multicenter, Week-wise-randomized, open-label, blinded-endpoint (PROBE) clinical trial comparing ultra-early prehospital blood pressure lowering delivered by a Mobile Stroke Unit (MSU) with standard Emergency Medical Services (EMS) in patients with spontaneous intracerebral hemorrhage.

NCT07641998 — Robot-Assisted Hematoma Evacuation With Intrahematoma Tenecteplase for Post-Reperfusion PH2 Hemorrhagic Transformation

StatusNot yet recruiting
PhasePhase 1
SponsorBeijing Tiantan Hospital
Enrollment20
Study TypeINTERVENTIONAL
ConditionsHemorrhagic Transformation Stroke
Interventions

The purpose of this phase I trial is to evaluate the safety and feasibility of robot-assisted stereotactic minimally invasive hematoma aspiration, followed when eligible by intrahematoma tenecteplase administration, in patients who develop symptomatic supratentorial PH2 hemorrhagic transformation after reperfusion therapy for acute ischemic stroke. The main study questions are whether this stra…

NCT07650110 — Biological Collection of the Rare Diseases of the Brain and Eye Vessels Cohort - 2

StatusNot yet recruiting
PhaseN/A
SponsorAssistance Publique - Hôpitaux de Paris
Enrollment600
Study TypeINTERVENTIONAL
ConditionsCADASIL; Cavernous Angioma; Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy; Small Vessel Disease
Interventions;

CERVCO is the French National Reference Centre for Rare Cerebrovascular and Retinal Diseases, accredited by the Ministry of Health since 2005. Since 2017, CERVCO has coordinated the MRVC cohort, a prospective cohort of patients with rare vascular diseases of the brain and retina, and established the associated B-MRVC biobank in 2020 to support translational research and biomarker discovery.

Du…

NCT06113939 — Prevention of Infection of the Respiratory Tract Through Application of Non-Invasive Methods of Secretion Suctioning

StatusNot yet recruiting
PhasePhase 4
SponsorHospital San Carlos, Madrid
Enrollment60
Study TypeINTERVENTIONAL
ConditionsIntubation Complication; Stroke, Ischemic; Stroke Hemorrhagic; Head Trauma; Cardiac Arrest
Interventions

Adults who are unconscious or severely ill and need a breathing tube connected to a ventilator are at high risk of developing a lung infection (pneumonia) within the first few days in the intensive care unit. This early pneumonia affects up to 30 to 50 % of certain high-risk patients, prolongs the time on the ventilator and in hospital, and increases the use of antibiotics.

Two strategies are …

NCT06696131 — Tenecteplase (TNK) in the Treatment of Intracerebral Hemorrhage (ICH)

StatusNot yet recruiting
PhasePhase 1
SponsorGaurav Gupta, MD
Enrollment5
Study TypeINTERVENTIONAL
ConditionsIntracerebral Hemorrhage; Intracranial Hemorrhages; Hemorrhagic Strokes
Interventions

The overall purpose of this study is to look at the safety and effectiveness of administering Tenecteplase (TNK) into the brain bleed (hematoma) instead of another clot-dissolving drug known as recombinant tissue plasminogen activator (rtPA), which is the current standard practice. Clot dissolving (Fibrinolytic) drugs work to break down blood clots and have been found to improve health outcomes…

NCT04157231 — Essential Acute Stroke Care in Low Resource Settings: a Pilot studY

StatusNot yet recruiting
PhaseN/A
SponsorThe George Institute
Enrollment300
Study TypeINTERVENTIONAL
ConditionsAcute Stroke
Interventions

An investigator-initiated, evaluator-blinded, prospective, multi centre, before-and-after, effectiveness-implementation hybrid design study to assess the feasibility of essential acute stroke care in a low resource setting

Enrolling by Invitation

NCT04534556 — Wireless Nerve Stimulation Device To Enhance Recovery After Stroke

StatusEnrolling by invitation
PhaseN/A
SponsorBaylor Research Institute
Enrollment42
Study TypeINTERVENTIONAL
ConditionsStroke; Chronic Stroke; Upper Extremity Paresis; Ischemic Stroke; Hemorrhagic Stroke
Interventions;

Texas Biomedical Device Center (TxBDC) has developed an innovative strategy to enhance recovery of motor and sensory function after neurological injury termed targeted plasticity therapy (TPT). This technique uses brief pulses of vagus nerve stimulation to engage pro-plasticity neuromodulatory circuits during rehabilitation exercises. Preclinical findings demonstrate that VNS paired with rehabi…

NCT05997914 — Storytelling for Reducing Gap in Anticoagulation Use in African Americans With Atrial Fibrillation

StatusEnrolling by invitation
PhaseN/A
SponsorUniversity of Massachusetts, Worcester
Enrollment80
Study TypeINTERVENTIONAL
ConditionsAtrial Fibrillation; Atrial Flutter; Adherence, Medication; Anticoagulants and Bleeding Disorders; Stroke
Interventions

The overall goal of this study is to evaluate the effectiveness of a previously developed storytelling intervention on anticoagulation (AC) initiation/persistence in African American and Black patients with atrial fibrillation/flutter. The investigators hope to gain knowledge that may help treat atrial fibrillation or flutter and lower stroke and adverse cardiovascular event risks for African A…

NCT07457333 — Beta-sitosterol for Subarachnoid Hemorrhage: Mechanistic Analysis of Recovery and Therapy

StatusEnrolling by invitation
PhasePhase 1 / Phase 2
SponsorSecond Affiliated Hospital, School of Medicine, Zhejiang University
Enrollment40
Study TypeINTERVENTIONAL
ConditionsSubarachnoid Haemorrhagic Stroke
Interventions;

Subarachnoid Hemorrhage (SAH), a devastating form of stroke, is associated with high mortality and disability rates due to complex secondary brain injuries-including neuroinflammation, oxidative stress, and blood-brain barrier disruption-for which effective neuroprotective treatments remain scarce. Inspired by the neuroprotective properties of the traditional Chinese herb Gastrodia elata, this …

NCT07681102 — Amplitude Modulation Frequency Comparison in Kilohertz Transcranial Magnetic Perturbation (kTMP) for Chronic Stroke

StatusEnrolling by invitation
PhaseN/A
SponsorMagnetic Tides
Enrollment7
Study TypeINTERVENTIONAL
ConditionsStroke
Interventions

Stroke is a leading cause of disability with many patients suffering chronic motor function impairments that affect their day-to-day activities. The goal of this proposal is to provide a first assessment of the feasibility and efficacy of an innovative non-invasive brain stimulation system, kTMP, in the treatment of motor impairment following stroke.

Completed Trials

NCT04038697 — Ischemic Conditioning Improves Walking Function Post Stroke

StatusCompleted
PhaseN/A
SponsorMedical College of Wisconsin
Enrollment132
Study TypeINTERVENTIONAL
ConditionsStroke; Stroke, Ischemic; Stroke Hemorrhagic; Stroke, Cardiovascular
Interventions; ;

This innovative study will address scientific and clinical areas relatively unexplored in chronic stroke that could lead to greater recovery of walking. Ischemic Conditioning (IC) is a non-invasive, simple procedure that improves motor function, exercise performance and cardiovascular function in healthy controls, but it has never been applied to the stroke population. We postulate that IC enha…

NCT04000971 — Coordinated, Collaborative, Comprehensive, Family-based, Integrated, Technology-enabled Stroke Care

StatusCompleted
PhaseN/A
SponsorVanderbilt University Medical Center
Enrollment1196
Study TypeINTERVENTIONAL
ConditionsStroke; Stroke, Ischemic; Stroke, Acute; Stroke Sequelae; Engagement, Patient
Interventions;

Stroke is the 5th leading cause of death and the leading cause of adult disability in the United States (US). Stroke is a complex disease with multiple interacting risk factors (including genetic, high blood pressure and cholesterol, and lifestyle factors like smoking, diet, and exercise) that lead to initial and recurrent stroke. Up to 90% of stroke survivors have some functional deficit that …

NCT05458908 — ProSPective Evaluation of Non-contrast sINe spiN Flat-dEtectoR CT for the Detection of Intracranial hemorrhageS

StatusCompleted
PhaseN/A
SponsorUniversity Hospital, Basel, Switzerland
Enrollment252
Study TypeINTERVENTIONAL
ConditionsStroke
Interventions;

Stroke is one of the leading causes of mortality and disability worldwide. Optimization of intra-hospital pathways is as of today one of the most promising research topics in stroke treatment. A potential solution to shorten the time needed for current workflows, and therefore reperfusion, is to do both imaging and subsequent endovascular therapy (EVT) in the angiography suite using non-contras…

NCT05671874 — Feasibility of a Digital Goals-of-Care Decision Aid for Clinicians and Families of Patients With SABI

StatusCompleted
PhaseN/A
SponsorUniversity of Massachusetts, Worcester
Enrollment50
Study TypeINTERVENTIONAL
ConditionsHemorrhagic Stroke, Intracerebral; Acute Ischemic Stroke; Traumatic Brain Injury
Interventions

The goal is to pilot test a highly accessible, web-based, pragmatic, scalable intervention to overcome ongoing problems with high stakes decision-making by surrogate decision-makers of patients in ICUs with severe acute brain injury (SABI), including those with moderate-severe traumatic brain injury, large hemispheric acute ischemic stroke and intracerebral hemorrhage.

NCT05675774 — DECT for Differentiating Intracerebral Hemorrhage From Contrast Extravasation

StatusCompleted
PhaseN/A
SponsorUniversity of Manitoba
Enrollment189
Study TypeINTERVENTIONAL
ConditionsStroke, Ischemic; Tomography, X-Ray Computed
Interventions

The goal of this clinical trial is to investigate the use of DECT (Dual-Energy Computed Tomography) in patients with acute ischemic stroke who receive an intervention (thrombolysis or thrombectomy). The main questions to answer are:

  1. Can DECT more accurately differentiate hyperdensities as intracranial haemorrhage (ICH) or contrast extravasation compared with single-energy CT (SECT)?.
  2. Wil…

NCT06134921 — Effects of Transcranial Electrical Stimulation in Stroke Individuals

StatusCompleted
PhaseN/A
SponsorMahidol University
Enrollment60
Study TypeINTERVENTIONAL
ConditionsIschemic Stroke; Hemorrhagic Stroke; Chronic Stroke; Subacute Stroke
Interventions; ;

The present study will use transcranial electrical stimulation (tES) with conventional physical therapy in sub-acute (at least 2 weeks after stroke onset) to chronic stroke within 2 years to investigate the effect on cortical activity and upper and lower limb motor function. The findings may support the usage of tES for improving brain activity and motor function in a clinic setting.

NCT07208422 — Task-Specific Self-Rehabilitation Training (TASSRET) Trial

StatusCompleted
PhaseN/A
SponsorNational Assembly Clinic
Enrollment50
Study TypeINTERVENTIONAL
ConditionsStroke; Stroke Hemorrhagic; Stroke Ischemic; Hemiparesis After Stroke
Interventions;

The goal of this pilot RCT is to evaluate the effectiveness of a Task-specific Self-rehabilitation Training (TASSRET) program and compare the effect of the two formats of the TASSRET (video vs manual) on functional ability (upper extremity fine and gross motor skills, upper extremity manual dexterity and speed, voluntary movement and basic mobility, gait velocity, balance) and health-related qu…

NCT06317194 — Pilot Study: A Novel Method of Non-Invasive Brain Stimulation (kTMP) to Enhance Motor Function in Chronic Stroke Patients

StatusCompleted
PhaseN/A
SponsorMagnetic Tides
Enrollment7
Study TypeINTERVENTIONAL
ConditionsStroke
Interventions

Stroke is a leading cause of disability with many patients suffering chronic motor function impairments that affect their day-to-day activities. The goal of this proposal is to provide a first assessment of the feasibility and efficacy of an innovative non-invasive brain stimulation system, kTMP, in the treatment of motor impairment following stroke.

Other (Suspended)

NCT05128513 — Delipid Extracorporeal Lipoprotein Filter From Plasma (DELP) for Acute Hemorrhagic Stroke

StatusSuspended
PhaseN/A
SponsorGeneral Hospital of Shenyang Military Region
Enrollment356
Study TypeINTERVENTIONAL
ConditionsHemorrhagic Stroke
Interventions

Delipid Extracorporeal Lipoprotein filter from Plasma (DELP) has been found to improve neurological function and life ability of AIS patients and approved for the treatment of AIS by China Food and Drug Administration (CFDA). A recent study imply that the neuroprotective effect of DELP involved multiple neuroprotective mechanism such as anti-inflammation, free radical scavenging, and decreasing…