Heredodegenerative Disorders, Nervous System: Clinical Trials

26 trials for Heredodegenerative Disorders, Nervous System, newest first

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26 active not recruiting. 26 Not applicable.

By phase and status

PhaseTrialsStatus
Not applicable26Active not recruiting 26

Follow Heredodegenerative Disorders, Nervous System: new trials by email Literature Review of Heredodegenerative Disorders, Nervous System trials Research Report on Heredodegenerative Disorders, Nervous System

Trials (filtered) newest first · largest first

All 26 trials

Tick up to 5 trials to compare them side by side (eligibility, arms, endpoints, adverse events) in a Literature Matrix.

TrialPhaseStatusSponsorEnrollmentStartUpdated
Effects of Whole-body Electrical Muscle Stimulation Exercise on Adults With Neuromuscular Disease
Whole-body Electrical Muscle Stimulation Exercise - Neuromuscular Diseases (NMD), Amyotrophic Lateral Sclerosis
Not applicableActive not recruitingUniversity of Missouri-Columbia502026-03-102026-11-06
Modification of Threat Interpretation Bias to Reduce Anxiety in Neurodegenerative Movement Disorders (Aim 3)
MindTrails-Movement, Waitlist Control - Huntington Disease, Parkinson Disease
Not applicableActive not recruitingUniversity of Virginia1362025-11-202026-07-20
Identification of Novel Biomarkers in Early Charcot-Marie-Tooth 1A Disease
Quantitative neuromuscular MRI, Skin biopsy, Clinical scores - Charcot-Marie-Tooth Disease Type 1A
Not applicableActive not recruitingAssistance Publique Hopitaux De Marseille552025-06-242026-10-28
Music Intervention for Brain-Heart Disease in Myotonic Dystrophy Type 1 (DM1)
Music and movement education - Myotonic Dystrophy, Congenital, Myotonic Dystrophy, Type 1 (DM1)
Not applicableActive not recruitingHanns Lochmuller132025-03-252026-07-28
Efficacy of Stabilometric Platform to Improve Standing Balance in Patients With Friedreich's Ataxia
Balance training over stabilometric platform, Balance training by means of conventional rehabilitation - Friedreich Ataxia
Not applicableActive not recruitingIRCCS Eugenio Medea242025-02-032026-11-05
Flexibility, Resistance, Aerobic, Movement Execution Training in Adults With Hereditary Spastic Paraplegia
Flexibility, Resistance, Aerobic, Movement Execution training - Hereditary Spastic Paraplegia
Not applicableActive not recruitingIRCCS Eugenio Medea202024-12-232026-11-05
Longitudinal SV2A PET and MRI in Premanifest HD
Diagnostic Test: 18F-SynVesT-1 PET, Volumetric MRI - Huntington Disease
Not applicableActive not recruitingUniversitaire Ziekenhuizen KU Leuven402024-12-042026-05-05
Diffrence in Thromboprofilaksis in Elderly Ostoepenic Hip Fractures According to Mobility Status by Genetic Analysis
Gene Expression Analysis - Hip Fracture of Intertrochanteric Type, Thromboembolic Event
Not applicableActive not recruitingSaglik Bilimleri Universitesi902024-11-012025-06-05
An Exploratory Study to Evaluate the Tolerability and Safety of MWAV201 in Subjects With Wilson Disease
MWAV201 - Wilson Disease
Not applicableActive not recruitingXinhua Hospital, Shanghai Jiao Tong University School of Medicine92024-10-282026-08-12
Enhancement of Quality of Work And Life
Preventive Participatory workplace intervention - Parkinson Disease, Hereditary Spastic Paraparesis
Not applicableActive not recruitingRadboud University Medical Center1242024-10-082026-08-14
Technology-supported Motor Rehabilitation for People With Rett Syndrome
computer gaming - Rett Syndrome
Not applicableActive not recruitingGeorgetown University142024-10-012026-10-28
Efficacy of tDCS in Degenerative Ataxia
transcranial direct current stimulation, Sham (No Treatment) - Ataxia, Cerebellar, Ataxia - Genetic Diagnosis - Unknown
Not applicableActive not recruitingUniversity of Cagliari162023-10-092025-11-26
Web Intervention for Parents of Youth With Genetic Syndromes (WINGS)
Functional Behavioral Training (FBT), Positive Parenting Strategies-Treatment as Usual - Telomeric 22Q13 Monosomy Syndrome, Tuberous Sclerosis
Not applicableActive not recruitingRush University Medical Center792023-09-152026-09-18
Promoting Goals-of-Care Discussions for Patients With Memory Problems and Their Caregivers
Jumpstart Guide - Dementia, Dementia, Vascular
Not applicableActive not recruitingUniversity of Washington18022023-09-112026-09-21
A Clinical Study Evaluating the Safety and Efficacy of SKG0201 Injection in Patients With Spinal Muscular Atrophy Type 1
SKG0201 Injection - Spinal Muscular Atrophy 1
Not applicableActive not recruitingKun Sun122023-06-252025-11-21
The Study of Transcranial Magnetic Stimulation in the Regulation of Spinocerebellar Ataxia
Transcranial magnetic stimulation - Spinocerebellar Ataxia
Not applicableActive not recruitingFirst Affiliated Hospital of Chongqing Medical University602023-05-012025-04-01
Tourette Deep Brain Stimulation (DBS) Target Detection & Suppression
Medtronic Percept Neurostimulator - Tourette Syndrome
Not applicableActive not recruitingUniversity of Florida82022-06-202026-09-25
Amyloidosis TTR Flow Reserve Evaluation
SPECT MPI - Amyloid Cardiomyopathy
Not applicableActive not recruitingCentre Hospitalier Régional d'Orléans502022-02-242025-12-23
A Remote Physical Activity Program in the Population Suffering from Type 1 Myotonic Dystrophy
Remote activity program - Myotonic Dystrophy Type 1 (DM1)
Not applicableActive not recruitingUniversité du Québec à Chicoutimi402021-08-112025-03-28
Measuring Impact of Computer Gaming on Arm Use in Rett Syndrome
Modified Virtual Reality Gaming - Rett Syndrome
Not applicableActive not recruitingGeorgetown University102021-05-012026-10-28

Showing 20 of 26. Sign in to see all of them.

Narrower conditions

Charcot-Marie-Tooth Disease (4)  ·  Huntington Disease (4)  ·  Parkinson Disease (4)  ·  Ataxia (3)  ·  Rett Syndrome (3)  ·  Spastic Paraplegia, Hereditary (3)  ·  Amyotrophic Lateral Sclerosis (2)  ·  Cerebellar Ataxia (2)  ·  Cerebral Palsy (2)  ·  Friedreich Ataxia (2)  ·  Hepatolenticular Degeneration (2)  ·  Muscular Atrophy, Spinal (2)  ·  Myotonic Dystrophy (2)  ·  Nervous System Diseases (2)  ·  Neuromuscular Diseases (2)

Broader conditions

Congenital, Hereditary, and Neonatal Diseases and Abnormalities (26)  ·  Genetic Diseases, Inborn (26)  ·  Nervous System Diseases (24)  ·  Neurodegenerative Diseases (23)  ·  Central Nervous System Diseases (16)  ·  Brain Diseases (14)  ·  Metabolic Diseases (10)  ·  Neurologic Manifestations (10)  ·  Neuromuscular Diseases (10)  ·  Nutritional and Metabolic Diseases (10)  ·  Pathological Conditions, Signs and Symptoms (10)  ·  Basal Ganglia Diseases (9)  ·  Movement Disorders (9)  ·  Peripheral Nervous System Diseases (9)

Interventions

Cognitive Behavioral Therapy (1)  ·  Gene Expression Profiling (1)  ·  Hematologic Tests (1)  ·  Pliability (1)  ·  Transcranial Direct Current Stimulation (1)  ·  Transcranial Magnetic Stimulation (1)

Sponsors

Assistance Publique Hopitaux De Marseille (2)  ·  Georgetown University (2)  ·  IRCCS Eugenio Medea (2)  ·  Burke Medical Research Institute (1)  ·  Centre Hospitalier Régional d'Orléans (1)  ·  Children's National Research Institute (1)  ·  First Affiliated Hospital of Chongqing Medical University (1)  ·  Hanns Lochmuller (1)  ·  InSightec (1)  ·  Kun Sun (1)  ·  Massachusetts General Hospital (1)  ·  Radboud University Medical Center (1)  ·  Rush University Medical Center (1)  ·  Saglik Bilimleri Universitesi (1)  ·  Thomas Jefferson University (1)

Countries

United States (11)  ·  Canada (3)  ·  China (3)  ·  France (3)  ·  Italy (3)  ·  Belgium (1)  ·  Netherlands (1)  ·  Turkey (Türkiye) (1)

Top investigators

Andres Lozano, MD (1)  ·  Aysegul Gunduz, PhD (1)  ·  Christopher Butson, PhD (1)  ·  Elbrich Postma, PhD (1)  ·  Elise Duchesne (1)  ·  Erin Kross, MD (1)  ·  Gabriella Paparella, Medical Degree (1)  ·  Jian-Gao Fan, doctor (1)  ·  Kathleen Friel (1)  ·  Kun Sun, Doctor (1)  ·  Leonardo Boccuni, PhD (1)  ·  Michael Okun, MD (1)  ·  Miriam Bornhorst, MD (1)

Results publications

PMID 28747452, PMID 32651242, PMID 35995551, PMID 36082269, PMID 36693691, PMID 37542335, PMID 37722831, PMID 40040914, PMID 40207026, PMID 41533249

NIH funding

K23NR020210 (1), R01AG078169 (1), UH3NS119844 (1)