Clinical Trials for Neurologic Diseases

Currently registered clinical trials for Neurologic Diseases from ClinicalTrials.gov. 23 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 Neurologic Diseases from the ClinicalTrials.gov database.

Trial Summary

  • Total studies: 50
  • Recruiting: 23
  • Active, not recruiting: 5
  • Completed: 16
  • Other: 6

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

Recruiting Trials

NCT00001248 — Magnetic Resonance Imaging (MRI) to Evaluate Activity of Multiple Sclerosis (MS)

StatusRecruiting
PhaseN/A
SponsorNational Institute of Neurological Disorders and Stroke (NINDS)
Enrollment3750
Study TypeOBSERVATIONAL
ConditionsMultiple Sclerosis

Studies performed under 89-N-0045 are designed to examine the natural history of multiple sclerosis (MS) using MRI and immunological measures. In addition to studying the natural history of untreated patients, the natural history of patients receiving approved disease-modifying therapies of MS will be examined. In both cohorts of patients levels of disease activity on MRI will be compared with …

NCT00001252 — Human Movement Database

StatusRecruiting
PhaseN/A
SponsorNational Institutes of Health Clinical Center (CC)
Enrollment7500
Study TypeOBSERVATIONAL
ConditionsMovement Disorder

This study will collect information on the different ways people control limb and body movements. This information will be used to develop a database on normal movements and adaptive movements of people who have diseases that affect the way they move. The database will serve as a tool to improve diagnosis and treatment of patients with movement-related problems.

Volunteers from one month old t…

NCT00001778 — Evaluation of Patients With HAM/TSP

StatusRecruiting
PhaseN/A
SponsorNational Institute of Neurological Disorders and Stroke (NINDS)
Enrollment750
Study TypeOBSERVATIONAL
ConditionsHTLV-I Infection; Tropical Spastic Paraparesis

Objective:

Human T-lymphotropic virus type-I-associated myelopathy / tropical spastic paraparesis (HAM/TSP) is a rare neurologic disorder that affects less than 5% of patients infected with the HTLV-I virus. The purpose of this protocol is to study the natural history of HAM/TSP by monitoring clinical progression of patients longitudinally. Additionally, we will attempt to define the virologic…

NCT05321017 — Wrist Extensor MEP Up-conditioning for Individuals With Incomplete Spinal Cord Injury

StatusRecruiting
PhaseN/A
SponsorMedical University of South Carolina
Enrollment5
Study TypeINTERVENTIONAL
ConditionsSpinal Cord Injuries; Quadriplegia
Interventions

The purpose of this study is to examine the relationship between common clinical assessments and measurements of the function of brain-spinal cord-muscle connections, and to examine the effects of training a brain-spinal cord-muscle response in individuals with incomplete spinal cord injury. A transcranial magnetic stimulator (TMS) is used for examining brain-to-muscle pathways. This stimulator…

NCT05518188 — Melpida: Recombinant Adeno-associated Virus (Serotype 9) Encoding a Codon Optimized Human AP4M1 Transgene (hAP4M1opt)

StatusRecruiting
PhasePhase 1 / Phase 2
SponsorElpida Therapeutics SPC
Enrollment4
Study TypeINTERVENTIONAL
ConditionsSpasticity, Muscle; Microcephaly; Intellectual Deficiency; Growth Retardation; SPG50
Interventions

MELPIDA is proposed for the treatment of subjects with SPG50 and targets neuronal cells to deliver a fully functional human AP4M1 cDNA copy via intrathecal injection to counter the associated neuronal loss. Outcomes will evaluate the safety and tolerability of a single dose of MELPIDA, which will be measured by the treatment-associated adverse events (AEs) and serious adverse events (SAEs). Sec…

NCT06154252 — RESET-Myositis: An Open-Label Study to Evaluate the Safety and Efficacy of CABA-201 in Subjects With Active Idiopathic Inflammatory Myopathy or Juvenile Idiopathic Inflammatory Myopathy

StatusRecruiting
PhasePhase 2 / Phase 3
SponsorCabaletta Bio
Enrollment74
Study TypeINTERVENTIONAL
ConditionsIdiopathic Inflammatory Myopathy; Dermatomyositis; Anti-Synthetase Syndrome; Immune-Mediated Necrotizing Myopathy; Juvenile Dermatomyositis
Interventions

RESET-Myositis: Open-Label Study to Evaluate the Safety and Efficacy of CABA-201 in Subjects with Active Idiopathic Inflammatory Myopathy or Juvenile Idiopathic Inflammatory Myopathy

NCT07690449 — Three CT Signs of Nerve-root Suffering in Low-back Sciatica: a Study of Their Frequency in Patients Referred for CT-guided Nerve-root Infiltration.

StatusRecruiting
PhaseN/A
SponsorCentre Hospitalier Universitaire de Nice
Enrollment400
Study TypeOBSERVATIONAL
ConditionsSciatica; Lumbosacral Radiculopathy; Low Back Pain
Interventions

Retrospective, observational, single-centre study conducted at Nice University Hospital (Pasteur 2), Department of Diagnostic and Interventional Radiology. Objective: to assess the prevalence of three CT signs sought next to the clinically suspected nerve root in patients with low-back sciatica referred for CT-guided foraminal/peri-radicular infiltration: (1) nerve-root size asymmetry/hypertrop…

NCT06352619 — Third Enhanced Control of Hypertension and Thrombectomy Stroke Domain Within ACT-GLOBAL Adaptive Platform Trial

StatusRecruiting
PhaseN/A
SponsorThe George Institute
Enrollment2000
Study TypeINTERVENTIONAL
ConditionsIschemic Stroke, Acute
Interventions; ;

Several clinical trials have produced variable conclusions regarding the effects of intensive blood pressure (BP) lowering in post-EVT acute ischaemic stroke (AIS) patients. Although two trials indicate harm from very intensive target-based treatment (SBP <130 mmHg), the others neutral effects in the SBP range 140-160 mmHg. The ENCHANTED3/MT domain of the ACT-GLOBAL platform trial aims to test…

NCT07656584 — Implementation of Communication Disability Collection and Accommodations in Primary Care Settings

StatusRecruiting
PhaseN/A
SponsorNYU Langone Health
Enrollment126870
Study TypeINTERVENTIONAL
ConditionsCommunication Disabilities
Interventions

This multi-methods-multi-site study aims to adapt and evaluate the effects of an implementation support package of strategies to assist primary care clinics in documenting patients’ communication disability (CD) and accommodation needs in the electronic health record (EHR) and providing communication accommodations through EHR data extraction, surveys, focus groups, interviews, and clinical pra…

NCT07174661 — Educational Tools for the Improvement of Early Advance Care Planning in Adolescents and Young Adults With Advanced Solid Tumors and High-Grade Brain Tumors

StatusRecruiting
PhaseN/A
SponsorMayo Clinic
Enrollment50
Study TypeINTERVENTIONAL
ConditionsAdvanced Malignant Solid Neoplasm; Malignant Brain Neoplasm; Recurrent Advanced Malignant Solid Neoplasm
Interventions; ;

This clinical trial studies whether educational tools work to improve early advance care planning (ACP) in adolescents and young adults (AYAs) with solid tumors that may have spread from where they first started to nearby tissue, lymph nodes, or distant parts of the body (advanced) and high-grade brain tumors. The incidence of AYA cancers is on the rise with approximately 90,000 new diagnoses y…

NCT07034794 — A Clinical Trial to Examine Lysoveta on Cognitive Function in Healthy Adults With Self-perceived Memory Problems

StatusRecruiting
PhaseN/A
SponsorAker BioMarine Human Ingredients AS
Enrollment138
Study TypeINTERVENTIONAL
ConditionsHealthy; Memory Problems
Interventions;

The study is a randomized, placebo-controlled, triple-blind, parallel group trial, in which the effect of krill oil is investigated in healthy volunteers with self-perceived memory problems. Volunteers are randomly allocated to the 2 study groups including placebo and Lysoveta. Over the whole study period, volunteers will be asked to complete questionnaires to evaluate cognitive performance and…

NCT07691411 — An Ecological Momentary Assessment Based Program to Support Self-Management for Post-stroke Patients

StatusRecruiting
PhaseN/A
SponsorThe Hong Kong Polytechnic University
Enrollment50
Study TypeINTERVENTIONAL
ConditionsStroke; Post Stroke
Interventions

The goal of this feasibility study is to test whether a new approach that combines real-time symptom tracking (Ecological Momentary Assessment) with machine learning can help people recovering from a stroke to better manage depression, thinking difficulties, and daily functioning. The main questions it aims to answer are:

Is this combined approach practical and acceptable for post-stroke survi…

NCT07689305 — Live Parent-Child Video Interaction and Cartoon Watching for Emergence Agitation in Children

StatusRecruiting
PhaseN/A
SponsorIzmir City Hospital
Enrollment150
Study TypeINTERVENTIONAL
ConditionsEmergence Delirium; Preoperative Anxiety
Interventions;

Preoperative anxiety is common in preschool-aged children and may make anesthesia induction more difficult and contribute to agitation during recovery from general anesthesia. Non-drug distraction methods may help children cope with separation from their parents and the unfamiliar operating room environment.

This single-center randomized controlled trial will include 150 children aged 2 to 6 y…

NCT07227974 — Empower EI: Comparing Early Intervention Approaches to Improve Communication in Toddlers With Developmental Delays

StatusRecruiting
PhaseN/A
SponsorNorthwestern University
Enrollment1269
Study TypeINTERVENTIONAL
ConditionsDevelopmental Delays
Interventions; ;

This study is testing three ways to deliver Early Intervention (EI) services for toddlers with developmental disabilities (DD).

Children enrolled in EI speech therapy will receive one of three approaches:

  1. Therapist Delivered EI: For 28 weeks, the child’s speech therapist will work directly with the child to support their communication.
  2. Caregiver Coaching EI: For 28 weeks, the child’s sp…

NCT07689331 — Hungarian National Systemic Amyloidosis Registry

StatusRecruiting
PhaseN/A
SponsorSemmelweis University
Enrollment300
Study TypeOBSERVATIONAL
ConditionsSystemic Amyloidosis; ATTR Amyloidosis; AL Amyloidosis; Amyloid Cardiomyopathy

This registry is an observational, multicenter, retrospective and prospective, non-pharmacological study designed to collect and analyze data from patients with systemic amyloidosis treated in inpatient and outpatient cardiology, hematology, nephrology, and neurology departments across Hungary. The registry was established in 2025.

NCT07235098 — Effect of a Music Intervention in Reducing Distress and Pain in Patients With Lung Cancer Undergoing Mini-invasive Surgery

StatusRecruiting
PhaseN/A
SponsorOncology Institute of Southern Switzerland
Enrollment74
Study TypeINTERVENTIONAL
ConditionsLung Cancer (Suspected or Confirmed)
Interventions

This study aims at evaluating whether music therapy intervention is effective in decreasing psychological (distress) and physical symptoms (pain) in patients with suspected or diagnosed lung cancer undergoing minimally invasive lung surgery.

NCT07054801 — IA Lidocaine and Methylprednisolone for Headache Associated With Subarachnoid Hemorrhage

StatusRecruiting
PhasePhase 2
SponsorDaniel Raper, MBBS
Enrollment25
Study TypeINTERVENTIONAL
ConditionsHeadaches Associated With Subarachnoid Hemorrhage (SAH)
Interventions;

Subarachnoid hemorrhage (SAH) is a type of bleeding around the brain that can cause sudden and severe headaches. These headaches can be debilitating and persist for weeks, significantly impacting a patient’s comfort and recovery. Many patients require opioids for pain control, which can lead to side effects such as drowsiness, constipation, and dependency. There is a need for new treatment stra…

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.

NCT07689396 — Predictors of Treatment Expectations in Myofascial Pain Syndrome

StatusRecruiting
PhaseN/A
SponsorKTO Karatay University
Enrollment85
Study TypeOBSERVATIONAL
ConditionsMyofascial Pain Syndromes

This cross-sectional study aims to determine the predictors of treatment expectations in individuals with myofascial pain syndrome (MPS). MPS is one of the most common causes of musculoskeletal pain and is associated with reduced quality of life. Patients’ pre-treatment expectations are known to influence clinical outcomes, yet the factors that predict these expectations have not been establish…

NCT07690670 — WhatsApp AI Support vs Paper Support for First-Time Hearing Aid Users

StatusRecruiting
PhaseN/A
SponsorUniversity of Pretoria
Enrollment66
Study TypeINTERVENTIONAL
ConditionsHearing Loss
Interventions; ;

The purpose of this study is to advance hearing care in low- and middle-income countries (LMICs) through the rigorous evaluation and optimization of innovative interventions and technologies. This study encompasses the following key aim:

This study aims to evaluate the effectiveness of a WhatsApp-delivered AI-enabled support and acclimatization programme for adults receiving preset hearing aid…

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…

NCT07416188 — Novel Indenoisoquinolone CMYC/TOPOISOMERASE 1 Inhibitor (LMP744) in Recurrent Glioblastoma

StatusRecruiting
PhasePhase 1 / Phase 2
SponsorNational Institute of Neurological Disorders and Stroke (NINDS)
Enrollment40
Study TypeINTERVENTIONAL
ConditionsRecurrent Glioblastoma; Glioblastoma IDH (Isocitrate Dehydrogenase) Wildtype; Relapsed Cancer; Recurrent Tumor; Glioblastoma Multiforme
Interventions;

Background:

Glioblastoma is a common brain cancer in adults. Treatment includes surgery, radiation, and chemotherapy. But this cancer can return after treatment and is often fatal. Researchers want to know if a study drug (LMP744) can kill glioblastoma tumor cells.

Objective:

To test LMP744 in people with glioblastoma.

Eligibility:

People aged 18 years or older with glioblastoma that retur…

NCT06615973 — Screening for Social Determinants of Health (SDOH) and Cognitive Function in Individuals With History of Stroke

StatusRecruiting
PhaseN/A
SponsorNational Institute of Neurological Disorders and Stroke (NINDS)
Enrollment450
Study TypeOBSERVATIONAL
ConditionsStroke; Brain Disease; Vascular Diseases; Cerebrovascular Disorder

Background:

Stroke is the fifth leading cause of death in the United States. It is also a leading cause of disability. More than 70% of people who survive strokes have mental impairment or dementia. Medical factors, such as the severity of the stroke, affect whether a person will have mental impairment afterward. But social factors, such as education and ethnicity, seem to play a role as well….

Active, Not Recruiting

NCT03726359 — Phase I Study of Fractionated Stereotactic Radiation Therapy

StatusActive, not recruiting
PhaseN/A
SponsorAlbert Einstein College of Medicine
Enrollment30
Study TypeINTERVENTIONAL
ConditionsBrain Metastases
Interventions

There is a lack of prospective trial data and consensus guidelines describing the use of Fractionated Stereotactic Radiation Therapy (FSRT) in the treatment of brain metastases. There has been no prospective dose escalation study performed to date to determine the maximum tolerated dose (MTD) in patients treated with FSRT. Prescription doses in the series described above ranged from 18 Gy to 42…

NCT05070858 — A Study to Test How Safe Pozelimab and Cemdisiran Combination Therapy and Cemdisiran Alone Are and How Well They Work in Adult Patients With Generalized Myasthenia Gravis

StatusActive, not recruiting
PhasePhase 3
SponsorRegeneron Pharmaceuticals
Enrollment288
Study TypeINTERVENTIONAL
ConditionsGeneralized Myasthenia Gravis
Interventions; ;

This study is researching the experimental drugs called pozelimab and cemdisiran, and cemdisiran monotherapy. The study is focused on patients with generalized Myasthenia Gravis (gMG). Myasthenia gravis is a disease that causes weakness and fatigue in muscles in the body because the nerves and muscles are not communicating properly.

The aim of the study is to see how effective pozelimab and ce…

NCT06094491 — Virtual Diabetes Group Visits Across Health Systems

StatusActive, not recruiting
PhaseN/A
SponsorUniversity of Chicago
Enrollment720
Study TypeINTERVENTIONAL
ConditionsT2DM (Type 2 Diabetes Mellitus); Hypertension; Heart Disease Chronic; Stroke; Hyperlipidemias
Interventions

The purpose of this project is to evaluate the effectiveness of a virtual diabetes group visits on patients with type 2 diabetes mellitus (T2DM).

NCT06659627 — Interventions Against Fatigue in Patients With Myasthenia Gravis

StatusActive, not recruiting
PhaseN/A
SponsorLeiden University Medical Center
Enrollment60
Study TypeINTERVENTIONAL
ConditionsMyasthenia Gravis; Fatigue
Interventions; ;

A prospective assessor-blinded randomized clinical trial investigating the effect of aerobic exercise therapy or cognitive behavioural therapy on fatigue in patients with myasthenia gravis.

NCT07406620 — Entropy-based Physiological Signal Analysis in Patients With Obstructive Sleep Apnoea

StatusActive, not recruiting
PhaseN/A
SponsorKing’s College London
Enrollment139
Study TypeOBSERVATIONAL
ConditionsObstructive Sleep Apnoea (OSA)
Interventions

This observational study is being undertaken as a part of a Master of Research (MRes) in Clinical Research programme.

Its goal is to learn about how continuous positive airway pressure (CPAP) therapy changes the complexity of body signals in adults with obstructive sleep apnoea (OSA). The main question it aims to answer is:

- How does the complexity of physiological signals (specifically oxy…

Not Yet Recruiting

NCT07691255 — MELanoma Brain Metastasis Treated With CYberknife

StatusNot yet recruiting
PhaseN/A
SponsorEuropean Institute of Oncology
Enrollment50
Study TypeOBSERVATIONAL
ConditionsMelanoma (Skin Cancer)

Melanoma is a type of cancer that can spread to the brain, making the disease harder to treat and worsening both survival and quality of life.

In recent years, treatments have improved significantly thanks to advances in surgery, radiotherapy, immunotherapy, and targeted therapy. These new treatments have greatly increased survival rates for patients with metastatic melanoma.

This study focus…

NCT06905470 — The Effects of Eccentric Compared to Standard Strength Training in Primary Spinal Cord Injury Rehabilitation

StatusNot yet recruiting
PhaseN/A
SponsorSwiss Paraplegic Research, Nottwil
Enrollment20
Study TypeINTERVENTIONAL
ConditionsSpinal Cord Injury
Interventions;

The goal of this clinical trial is to assess the effects of eccentric arm-crank (KREHA) training compared to standard clinical routine strength (STAN) training in individuals undergoing primary spinal cord injury (SCI) rehabilitation.

The main questions this trail aims to answer are:

  • what are the effects of the training on upper body strength, aerobic performance, muscle volume, functional …

NCT07361627 — Upper Limb Rehabilitation Using Non-invasive Spinal Cord Stimulation

StatusNot yet recruiting
PhaseN/A
SponsorCentre for Interdisciplinary Research in Rehabilitation of Greater Montreal
Enrollment40
Study TypeINTERVENTIONAL
ConditionsSpinal Cord Injury Cervical; Spinal Cord Injury, Acute; Spinal Cord Injury (Quadraplegia)
Interventions;

The goal of this RCT study is to evaluate if combining activity-based therapy (ABT) with transcutaneous spinal cord stimulation (tSCS) can improve recovery of arm and hand movement in people with cervical spinal cord injury (SCI). As secondary aims, the study will also investigate at how this combination approach affects the cortical changes in the somatosensory and motor areas of the brain, as…

NCT07129759 — Phase 3 Long Term Safety Extension Study of LUM-201 in Children With Growth Hormone Deficiency

StatusNot yet recruiting
PhasePhase 3
SponsorLumos Pharma
Enrollment150
Study TypeINTERVENTIONAL
ConditionsGrowth Hormone Deficiency (GHD)
Interventions

This is a Multi-national Trial. The Goal of the Trial is to Offer Subjects Who Complete 12 Months in the LUM-201-10 Phase 3 Trial up to an Additional 36 Months of Treatment of LUM-201 While Evaluating Safety and Tolerability of LUM-201.

Enrolling by Invitation

NCT05350774 — Immunotherapy for Neurological Post-Acute Sequelae of SARS-CoV-2

StatusEnrolling by invitation
PhasePhase 2
SponsorNational Institute of Neurological Disorders and Stroke (NINDS)
Enrollment45
Study TypeINTERVENTIONAL
ConditionsSystemic Inflammation; Neuroinflammation; Microvascular Thrombosis
Interventions;

Background:

COVID-19 can cause problems in different parts of the body. For most people, it causes fevers or trouble breathing. Some people might not recover all the way. Researchers want to see if a treatment can help with people who have recovered from COVID-19 but still have symptoms (“Long COVID”).

Objective:

To learn if human immunoglobulin (IVIG) will help with neurological symptoms of…

NCT07149428 — Longitudinal Deep Phenotyping of Central Mechanisms in Dysosmia: A Pilot Study Using Electrobulbogram (EBG), Functional MRI (fMRI), and Diffusion-Weighted Imaging (DWI)

StatusEnrolling by invitation
PhaseN/A
SponsorNational Institute on Deafness and Other Communication Disorders (NIDCD)
Enrollment80
Study TypeOBSERVATIONAL
ConditionsRespiratory Tract Infection; Smell Disorder; Influenza; Rhinosinusitis; COVID-19

Background:

Loss of the sense of smell can seriously affect a person’s quality of life. The ability to smell can be damaged by many factors, including illnesses, injuries, and exposure to toxic chemicals. The effects can vary, including complete loss of smell, partial loss, and parosomia, which is when things smell differently than they should.

Objective:

To study how brain function changes …

Completed Trials

NCT00001813 — Examination of Clinical and Laboratory Abnormalities in Patients With Defective DNA Repair: Xeroderma Pigmentosum, Cockayne Syndrome, or Trichothiodystrophy

StatusCompleted
PhaseN/A
SponsorNational Cancer Institute (NCI)
Enrollment709
Study TypeOBSERVATIONAL
ConditionsCockayne Syndrome; Skin Neoplasms; Xeroderma Pigmentosum; Trichothiodystrophy Syndromes; Genodermatosis

Four rare genetic diseases, xeroderma pigmentosum (XP), Cockayne syndrome (CS), the XP/CS complex and trichothiodystrophy (TTD) have defective DNA excision repair although only XP has increased cancer susceptibility. We plan to perform careful clinical examination of selected patients with XP, XP/CS, CS, or TTD and follow their clinical course. We will obtain tissue (skin, blood, hair, buccal s…

NCT00023036 — Clinical and Genetic Analysis of Enlarged Vestibular Aqueducts

StatusCompleted
PhaseN/A
SponsorNational Institute on Deafness and Other Communication Disorders (NIDCD)
Enrollment324
Study TypeOBSERVATIONAL
ConditionsSensorineural Hearing Loss; Cytomegalovirus Infection

This study will try to identify and understand the genetic factors that lead to an inner ear malformation called “enlarged vestibular aqueducts”, that can be associated with hearing loss.

Patients with sensorineural hearing loss with or without inner ear malformations and their parents and siblings may be eligible for this study. Participants and their immediate family members, may undergo som…

NCT01132937 — Evaluation, Pathogenesis, and Outcome of Subjects With or Suspected Traumatic Brain Injury

StatusCompleted
PhaseN/A
SponsorNational Institute of Neurological Disorders and Stroke (NINDS)
Enrollment886
Study TypeOBSERVATIONAL
ConditionsTraumatic Brain Injury

Background:

- Traumatic brain injury may have a range of effects, from severe and permanent disability to more subtle functional and cognitive deficits that often go undetected during initial treatment. To improve treatments and therapies and to provide a uniform quality of care, researchers are interested in developing more standardized criteria for diagnosing and classifying different types…

NCT01498263 — Inherited Diseases, Caregiving, and Social Networks

StatusCompleted
PhaseN/A
SponsorNational Human Genome Research Institute (NHGRI)
Enrollment682
Study TypeOBSERVATIONAL
ConditionsUndiagnosed Disease; Healthy Volunteer (Adult With Typically Developing Child); Inherited Neurodegenerative Disorders; Inherited Metabolic Disorders (Inborn Errors of Metabolism); Alzheimer’s Disease and Related Dementias

Approximately 66 million informal caregivers care for someone who is ill, disabled, or aged. These caregivers experience significant distress associated with caregiving, which may be particularly salient in the context of inherited conditions. Previous studies have not examined caregiving from a network perspective, nor have they considered how cognitive and emotional responses, such as caregiv…

NCT01947907 — Safety, PK/PD (Pharmacokinetics/Pharmacodynamics) and Efficacy of ACP-001 Weekly Versus Daily hGH in Children With Growth Hormone Deficiency (GHD)

StatusCompleted
PhasePhase 2
SponsorAscendis Pharma A/S
Enrollment53
Study TypeINTERVENTIONAL
ConditionsGrowth Hormone Deficiency (GHD)
Interventions;

A six month study of ACP-001, a long-acting growth hormone product, versus standard human growth hormone therapy. ACP-001 will be given once-a-week, standard human growth hormone (hGH) will be given on a daily basis. The primary aim is to demonstrate safety, pharmacokinetics and pharmacodynamics over a period of six months. A secondary objective is the comparison of height velocity (HV) of the …

NCT02694783 — Adoptive Cellular Immunotherapy for Progressive Multifocal Leukoencephalopathy With Ex Vivo Generated Polyomavirus-Specific T-Cells

StatusCompleted
PhaseEarly Phase 1
SponsorNational Institute of Neurological Disorders and Stroke (NINDS)
Enrollment60
Study TypeINTERVENTIONAL
ConditionsProgressive Multifocal Leukoencephalopathy
Interventions

Background:

Progressive Multifocal Leukoencephalopathy (PML) is a brain infection in people with a weakened immune system. Researchers think polyoma virus specific T cells (PyVST) therapy can treat PML. The PyVST cells are made from blood cells of a healthy relative. They are grown in a lab to expand the virus-killing cells, then given to the person with PML.

Objective:

To test whether PyVST…

NCT02669225 — Brain Amyloid- Retention During Wakefulness and Following Emergence From Sleep in Healthy People

StatusCompleted
PhaseEarly Phase 1
SponsorNational Institute on Alcohol Abuse and Alcoholism (NIAAA)
Enrollment22
Study TypeINTERVENTIONAL
ConditionsNormal Physiology
Interventions

Background:

Brain activity creates waste products. The body s glymphatic system removes this waste, especially during sleep. One brain waste product is amyloid-beta (Ab). It plays a role in Alzheimer s disease. Researchers want to study the effect of sleep on Ab in the brain.

Objective:

To see if sleep affects the amount of waste product removed from the brain.

Eligibility:

Healthy people …

NCT03251989 — Rare CNS Tumors Outcomes &Risk

StatusCompleted
PhaseN/A
SponsorNational Cancer Institute (NCI)
Enrollment326
Study TypeOBSERVATIONAL
ConditionsHigh Grade Meningioma; Ependymoma; Medulloblastoma; PNET; Primary CNS Sarcoma

Background:

Primary tumors of the brain and spine are those that start in the brain or spine. These tumors are rare, accounting for <2% of all cancers diagnosed in the United States. Some of these tumors occur in less than 2,000 people per year. Researchers want to study a large group of people with this kind of tumor. They want to learn more about the tumors, including the risk factors relat…

NCT07689617 — Ultrasound-Guided Intermediate Cervical Plexus Block for Postoperative Analgesia in Vagus Nerve Stimulation Surgery

StatusCompleted
PhaseN/A
SponsorFirat University
Enrollment52
Study TypeINTERVENTIONAL
ConditionsDrug-Resistant Epilepsy; Epilepsy; Vagus Nerve Stimulation
Interventions; ;

This prospective, randomized, double-blind, placebo-controlled clinical trial aims to evaluate the analgesic efficacy of ultrasound-guided intermediate cervical plexus block (ICB) in patients undergoing vagus nerve stimulation (VNS) implantation surgery under general anesthesia. Participants are randomly assigned to receive either an ultrasound-guided ICB with 10 mL of 0.25% bupivacaine or a pl…

NCT05559398 — Glenzocimab for REperfusion in the Setting of Endovascular Therapy for Brain infarctioN: GREEN Study

StatusCompleted
PhasePhase 2 / Phase 3
SponsorAssistance Publique - Hôpitaux de Paris
Enrollment108
Study TypeINTERVENTIONAL
ConditionsStroke, Acute; Stroke, Ischemic
Interventions;

Emergent reperfusion is the main goal for acute ischemic stroke therapy (AIS). Endovascular therapy (EVT) is recommended within 6 hrs of stroke onset, and up to 24 hrs following perfusion imaging criteria.

Despite the major benefit associated with MT, more than 50% of the patients remain disabled at 3 months. Reperfusion rates after MT are critical to determine functional outcome. However, com…

NCT05397353 — Sleep Treatment for Teens

StatusCompleted
PhaseN/A
SponsorRutgers, The State University of New Jersey
Enrollment12
Study TypeINTERVENTIONAL
ConditionsSleep Problem; Suicidal Ideation; Suicide, Attempted
Interventions

The purpose of this research study is to test a brief (6-session), empirically supported, and highly disseminable version of digital (i.e., smartphone or web-based) cognitive behavioral therapy for insomnia (dCBT-I), called SleepioTM, in suicidal adolescents with co-occurring insomnia during the high-risk post-hospitalization period. Suicide is the 2nd leading cause of death among adolescents. …

NCT06578780 — Design and Delivery Preferences for Exercise Intervention in People With Spinal Cord Injury

StatusCompleted
PhaseN/A
SponsorUniversity of Alabama at Birmingham
Enrollment110
Study TypeOBSERVATIONAL
ConditionsSpinal Cord Injuries

This research study aims to explore people’s understanding of physical activity behavior and perceptions of what a physical activity program should include for supporting initiation and continuous participation. This study will enroll up to 30 adults (18 or over) with spinal cord injury. The study will use a discrete choice experiment (DCE) design that implements both quantitative (development …

NCT06983600 — The Effect of SuJok Application on Dysmenorrhea and Quality of Life in Young People With Primary Dysmenorrhea:

StatusCompleted
PhaseN/A
SponsorMuş Alparslan University
Enrollment100
Study TypeINTERVENTIONAL
ConditionsDysmenorrhea (Disorder); Alternative Treatment
Interventions

Menarche, which is one of the most prominent features of maturation in adolescents and the transition from childhood to adulthood, causes many problems. The most prominent of these complaints is dysmenorrhea. Primary dysmenorrhea, the most common form of dysmenorrhea, is a gynecological disorder characterized by pain that starts in the lower abdomen before or during menstruation and radiates to…

NCT06811129 — Long-Term Neurologic and Neurocognitive Sequelae Following Pediatric Ebola Virus in Liberia

StatusCompleted
PhaseN/A
SponsorNational Institute of Neurological Disorders and Stroke (NINDS)
Enrollment328
Study TypeOBSERVATIONAL
ConditionsEbola; Post-Acute Ebola Syndrome

Background:

Ebola virus disease (EVD) causes fever, vomiting, and diarrhea, and may cause internal bleeding. It is often fatal. EVD may also damage the brain and nervous system. It can cause headaches, tremors, weakness, and other problems. These issues can continue for years after people recover from EVD infection. Researchers want to understand more about how EVD may have affected the brains…

NCT07689084 — Training Program to Improve EEG Competence

StatusCompleted
PhaseN/A
SponsorUniversity Hospital Marburg
Enrollment18
Study TypeINTERVENTIONAL
ConditionsEpilepsy; Status Epilepticus; Status Epilepticus, Electrographic; Status Epilepticus, Non-Convulsive; Healthy
Interventions

The goal of this clinical trial is to investigate the extent to which a practice-oriented training program for intensive care nursing staff and non-physician treatment teams can contribute to the earlier detection of epileptic seizures, with particular emphasis on SE.

Further objectives include enhancing competence in EEG interpretation and minimizing existing communication and procedural barr…

NCT07335822 — The Effectiveness of Low-Level Laser Therapy in the Treatment of Meralgia Paresthetica

StatusCompleted
PhaseN/A
SponsorIstanbul Training and Research Hospital
Enrollment36
Study TypeINTERVENTIONAL
ConditionsMeralgia Paresthetica; Lateral Femoral Cutaneous Nerve Entrapment
Interventions;

Patients diagnosed with meralgia paresthetica via electromyography (EMG), who present with neuropathic complaints on the lateral thigh to the Physical Medicine and Rehabilitation outpatient clinics of our hospital, will be included in the study after reviewing exclusion criteria. Patients will be randomized into two equal groups using a sealed-envelope system. The treatment group will receive l…