Clinical Trials for Autonomic Nervous System Disorders

Currently registered clinical trials for Autonomic Nervous System Disorders from ClinicalTrials.gov. 25 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 Autonomic Nervous System Disorders from the ClinicalTrials.gov database.

Trial Summary

  • Total studies: 50
  • Recruiting: 25
  • Active, not recruiting: 9
  • Completed: 9
  • Other: 7

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

Recruiting Trials

NCT02795052 — Neurologic Stem Cell Treatment Study

StatusRecruiting
PhaseN/A
SponsorMD Stem Cells
Enrollment500
Study TypeINTERVENTIONAL
ConditionsNeurologic Disorders; Nervous System Diseases; Neurodegenerative Diseases; Neurological Disorders; Stroke
Interventions

This is a human clinical study involving the isolation of autologous bone marrow derived stem cells (BMSC) and transfer to the vascular system and inferior 1/3 of the nasal passages in order to determine if such a treatment will provide improvement in neurologic function for patients with certain neurologic conditions. http://mdstemcells.com/nest/

NCT03137472 — TMS for Complex Regional Pain Syndrome

StatusRecruiting
PhaseN/A
SponsorStanford University
Enrollment40
Study TypeINTERVENTIONAL
ConditionsComplex Regional Pain Syndromes
Interventions

The aim of the current study is to assess the efficacy of TMS in the treatment of Complex Regional Pain Syndrome (CRPS). It is hypothesized that participants who receive TMS (Group 1) relative to sham treatment (Group 2) once daily for two days will demonstrate a greater improvement in CRPS-related pain and other associated symptomology (i.e., cognitive, emotional and physical) compared to base…

NCT04782830 — Use of Accelerometer for Quantification of Neurogenic Orthostatic Hypotension Symptoms

StatusRecruiting
PhaseN/A
SponsorVanderbilt University Medical Center
Enrollment29
Study TypeINTERVENTIONAL
ConditionsOrthostatic; Hypotension, Neurogenic; Autonomic Failure; Pure Autonomic Failure; Multiple System Atrophy; Orthostatic; Hypotension, Parkinsonism
Interventions; ;

The objective of this study is to find a more objective and accurate way to assess the efficacy of the treatment for neurogenic orthostatic hypotension. For this purpose, the investigators will use an activity monitor to determine the amount of time patients spend in the upright position (standing and walking; upright time) during 1 week of placebo (a pill with no active ingredients) and 1 week…

NCT05107635 — Inappropriate Sinus Tachycardia Registry

StatusRecruiting
PhaseN/A
SponsorAtriCure, Inc.
Enrollment500
Study TypeOBSERVATIONAL
ConditionsInappropriate Sinus Tachycardia; Postural Tachycardia Syndrome
Interventions

The primary objective of this registry is to capture real-world safety and performance data on AtriCure devices used to ablate cardiac tissue when treating Inappropriate Sinus Tachycardia (IST) or Postural Tachycardia Syndrome (POTS). This is a retrospective and prospective, multicenter, US/OUS, observational data registry.

NCT04645160 — Evaluating Efficacy of Tivozanib (AV-951) in Biliary Tract Cancers

StatusRecruiting
PhasePhase 1 / Phase 2
SponsorNational Cancer Institute (NCI)
Enrollment31
Study TypeINTERVENTIONAL
ConditionsCholangiocarcinoma; Bile Duct Neoplasm; Biliary Tract Malignancy
Interventions

Background:

Cholangiocarcinoma (CCA) is an aggressive cancer of the bile ducts. People with CCA have few treatment options and poor survival. Researchers want to see if a new drug can stop or slow CCA growth.

Objective:

To find the safest and most effective dose of tivozanib to treat CCA and learn its overall response rate.

Eligibility:

Adults ages 18 and older with CCA not removable with …

NCT05768139 — First-in-Human Study of Tersolisib (STX-478) as Monotherapy and in Combination With Other Antineoplastic Agents in Participants With Advanced Solid Tumors

StatusRecruiting
PhasePhase 1 / Phase 2
SponsorEli Lilly and Company
Enrollment880
Study TypeINTERVENTIONAL
ConditionsBreast Cancer; Solid Tumors, Adult
Interventions; ;

Study STX-478-101 (LY4064809) is a multipart, open-label, phase 1/2 study evaluating the safety, tolerability, pharmacokinetics (PK), and preliminary antitumor activity of STX-478 (LY4064809) in participants with advanced solid tumors with P13Ka mutations.

Part 1 will evaluate STX-478 as monotherapy in participants with advanced solid tumors. Part 2 will evaluate STX-478 therapy as combination…

NCT07671625 — Comprehensive Perioperative Program Based on Prehabilitation, Nutritional Intervention and Psychological Support for Patients With Locally Advanced Operable Oesophagogastric Cancer

StatusRecruiting
PhaseN/A
SponsorMasaryk Memorial Cancer Institute
Enrollment60
Study TypeINTERVENTIONAL
ConditionsLocally Advanced Esophageal Cancer; Gastroesophageal Junction Cancer; Gastric Cancer
Interventions; ;

Perioperative chemotherapy (CHT) or CHT/RT combined with surgery is the standard therapeutic approach for the treatment of locally advanced cancer of the esophagus, gastroesophageal junction (GEJ), and stomach. Comprehensive cancer treatment is associated with high perioperative morbidity and mortality. Serious postoperative complications occur in up to 20-80% of patients undergoing esophagecto…

NCT05689944 — Dance-therapy and Chronic Pain

StatusRecruiting
PhaseN/A
SponsorHospices Civils de Lyon
Enrollment160
Study TypeINTERVENTIONAL
ConditionsChronic Pain; Complex Regional Pain Syndromes; Tension-Type Headache
Interventions; ;

Pain, when it becomes chronic, can be a threat to patients and it is very common to observe a fear of pain and a fear of movement (kinesiophobia). Avoidance of movement due to fear of pain can lead to a deterioration of body image. Non-medicinal therapies are essential to correct this fear and movement avoidance behavior, to decrease “catastrophic” judgments and thus anxiety. The use of art-the…

NCT07689214 — Normast3 for Adults With Diabetic Polyneuropathy

StatusRecruiting
PhaseN/A
SponsorUniversity of Roma La Sapienza
Enrollment40
Study TypeINTERVENTIONAL
ConditionsDiabete Type 2
Interventions;

The goal of this clinical trial is to find out if a new supplement called Normast® 3 can help reduce nerve pain and improve nerve function in adults with diabetic polyneuropathy (DPN). DPN is a common complication of diabetes that damages nerves, often causing burning, tingling, or stabbing pain, as well as problems with the autonomic nervous system, which controls things like sweating and hear…

NCT07671898 — Comparison of Focal Cryoablation vs. Radiofrequency Cardioneuroablation for Bradyarrhythmias

StatusRecruiting
PhaseN/A
SponsorTomsk National Research Medical Center of the Russian Academy of Sciences
Enrollment60
Study TypeINTERVENTIONAL
ConditionsBradycardia; Syncope, Vasovagal; Sick Sinus Syndrome; Atrioventricular Block
Interventions;

Bradyarrhythmias are conditions where the heart beats too slowly, causing symptoms like dizziness, fainting, and fatigue. In some patients, these slow heart rhythms are caused by overactivity of the vagus nerve (the part of the nervous system that slows the heart down).

Cardioneuroablation (CNA) is a catheter-based procedure that targets and reduces the effect of these overactive nerves on the…

NCT06841198 — Cardiovascular Function and Response to Stimulation Within the First Year After Spinal Cord Injury

StatusRecruiting
PhaseN/A
SponsorKessler Foundation
Enrollment15
Study TypeINTERVENTIONAL
ConditionsSpinal Cord Injuries (SCI); Orthostatic Hypotension, Dysautonomic; Cardiovascular; Transcutaneous Spinal Stimulation
Interventions;

The study aims to explore how cardiovascular function changes in the first year after a spinal cord injury, and to see how different treatments, like spinal stimulation through the skin (transcutaneous spinal stimulation), affect blood pressure.

The main questions are:

How does stimulation affect blood pressure over the year? What is the level of cardiovascular activation throughout the year?…

NCT06993844 — Phase 1/2 Study of ETX-636 in Participants With Advanced Solid Tumors

StatusRecruiting
PhasePhase 1 / Phase 2
SponsorEnsem Therapeutics
Enrollment233
Study TypeINTERVENTIONAL
ConditionsAdvanced Solid Tumors; Advanced Breast Cancer
Interventions; ;

Phase 1/2, open-label study of ETX-636 in participants with advanced solid tumors

NCT06920134 — Epidural Electrical Stimulation to Support Hemodynamic Management in Individuals With Parkinson’s Disease

StatusRecruiting
PhaseN/A
SponsorEcole Polytechnique Fédérale de Lausanne
Enrollment5
Study TypeINTERVENTIONAL
ConditionsHypotension Symptomatic; Parkinson’s Disease; Orthostatic Hypotension, Dysautonomic; Multiple System Atrophy (MSA) With Orthostatic Hypotension; Multiple System Atrophy - Parkinsonian Subtype (MSA-P)
Interventions

The PD-HemON study aims to evaluate the safety and preliminary efficacy of ARC-IM Therapy (Epidural Electrical Stimulation) to support hemodynamic management in people with typical and atypical Parkinson’s Disease, who suffer from orthostatic hypotension.

NCT07197866 — An Extension Trial to Test if TEV-56286 is Effective in Relieving Multiple System Atrophy

StatusRecruiting
PhasePhase 2
SponsorTeva Branded Pharmaceutical Products R&D LLC
Enrollment200
Study TypeINTERVENTIONAL
ConditionsMultiple System Atrophy
Interventions

The primary objective of the trial is to describe the long-term safety and tolerability of TEV-56286 administered orally for the treatment of adult participants with Multiple System Atrophy (MSA).

A secondary objective of the trial is to further describe the safety and tolerability of TEV-56286.

The planned total duration of the trial is approximately 100 weeks.

NCT07143669 — Screening Study for KIT D816V Mutated Mast Cell Disease in Select Populations

StatusRecruiting
PhaseN/A
SponsorBlueprint Medicines Corporation
Enrollment450
Study TypeOBSERVATIONAL
ConditionsClonal Mast Cell Disease; KIT D816V Mutation; Suspected KITD816V Mutated Clonal Mast Cell Disease
Interventions

This is a multicenter screening study to characterize the prevalence of the KIT D816V mutation in participants with suspected clonal mast cell disease.

NCT07233278 — High-Intensity, Low-Frequency Periodic rTMS Over the Right Dorsolateral Prefrontal Cortex on Cardiac Autonomic Regulation in Women With Recurrent Pregnancy Loss and Anxiety

StatusRecruiting
PhaseN/A
SponsorShenyang Medical College
Enrollment48
Study TypeINTERVENTIONAL
ConditionsRecurrent Pregnancy Loss(RPL); Anxiety
Interventions;

The goal of this clinical trial is to determine whether high-intensity, low-frequency periodic repetitive transcranial magnetic stimulation (rTMS) applied to the right dorsolateral prefrontal cortex (DLPFC) can modulate cardiac autonomic regulation in women with recurrent pregnancy loss (RPL) and comorbid anxiety. The main questions it aims to answer are:

Does 120% resting motor threshold (RMT…

NCT07570212 — Individualized Transcranial Magnetic Stimulation in Parkinsonian Disorders

StatusRecruiting
PhaseN/A
SponsorPeking University First Hospital
Enrollment50
Study TypeINTERVENTIONAL
ConditionsParkinson’s Disease; Multiple System Atrophy; Progressive Supranuclear Palsy
Interventions

This clinical trial aims to evaluate whether individualized targeted repetitive transcranial magnetic stimulation (rTMS) can improve motor and non-motor symptoms in patients with parkinsonian disorders. The main question it aims to answer is:

  • Does individualized targeted rTMS alleviate symptoms of parkinsonian disorders?
  • Which clinical manifestations of parkinsonian syndromes are responsiv…

NCT07482501 — Repetitive Transcranial Magnetic Stimulation in Cardiac Autonomic Dysfunction

StatusRecruiting
PhaseN/A
SponsorAfyonkarahisar Health Sciences University
Enrollment44
Study TypeINTERVENTIONAL
ConditionsStroke; Autonomic Dysfunction; Hemiparesis
Interventions;

The aim of this study is to investigate the effects of repetitive transcranial magnetic stimulation (rTMS) added to conventional neurological rehabilitation on heart rate variability (HRV), quality of life, upper extremity muscle strength and autonomic symptoms in patients with stroke.

NCT07361692 — Effectiveness of Transcranial Direct Current Stimulation (tDCS) in the Management of Complex Regional Pain Syndrome

StatusRecruiting
PhaseN/A
SponsorPolyclinique de l’Europe
Enrollment32
Study TypeINTERVENTIONAL
ConditionsComplex Regional Pain Syndrome (CRPS)
Interventions;

Transcranial direct current stimulation (tDCS) is a non-invasive therapy increasingly used in facilities treating patients with chronic pain. This complementary therapy has the advantage of being non-pharmacological, with transient and mild side effects, an excellent safety profile, and good efficacy in the contexts where it has been the subject of dedicated research: neuropathic pain, fibromya…

NCT07210515 — Evaluation of IV AMBTX-01 (Neridronate) for Treatment of CRPS Type 1 (CRPS-RISE)

StatusRecruiting
PhasePhase 3
SponsorAmbros Therapeutics, Inc.
Enrollment270
Study TypeINTERVENTIONAL
ConditionsComplex Regional Pain Syndrome Type I
Interventions;

Phase 3 Trial of AMBTX-01 (neridronate) for Complex Regional Pain Syndrome Type 1

NCT07558733 — Sapanisertib and Serabelisib (PIKTOR) in Various Combinations in Patients With HR+/HER2- Advanced/Metastatic Breast Cancer

StatusRecruiting
PhasePhase 1 / Phase 2
SponsorFaeth Therapeutics
Enrollment32
Study TypeINTERVENTIONAL
ConditionsHR+ HER2- Breast Cancer
Interventions; ;

The study is a Phase 1b/2, multi-center, open-label, dose escalation trial evaluating the safety and preliminary efficacy of sapanisertib and serabelisib (PIKTOR) with fulvestrant and/or other anticancer therapies in participants with HR+/HER2- advanced/metastatic breast cancer.

NCT07348783 — Yogabased Movements for Primary Headaches (Migraine and/or Cluster Headache) - YOURHEAD

StatusRecruiting
PhaseN/A
SponsorKarolinska Institutet
Enrollment80
Study TypeINTERVENTIONAL
ConditionsCluster Headache - Episodic and Chronic; Migraine Headache; Migraine Headache, With or Without Aura; Migraine in Adults; Cluster Headaches and Other Trigeminal Autonomic Cephalgias
Interventions

Brief Summary:

Migraine and/or Cluster Headache: Study Overview

**Background:** Migraine and cluster headache are two primary headache disorders that significantly impact quality of life and functionality in those affected. According to the WHO’s recurring burden of disease reports, migraine is among the neurological conditions responsible for the highest number of years lost due to illne…

NCT07677137 — A First-in-human Study to Assess the Initial Safety, Tolerability, and Effectiveness of the ONSS Bilateral Occipital Nerve Field Stimulation System for the Prophylactic Treatment of Chronic Cluster Headache in Difficult-to-treat Subjects.

StatusRecruiting
PhaseN/A
SponsorMan and Science, SA
Enrollment10
Study TypeINTERVENTIONAL
ConditionsChronic Cluster Headache
Interventions

The purpose of this clinical trial is to evaluate the safety and effectiveness of the Occipital Nerve Stimulation System (ONSS) in treating chronic cluster headache in adults.

The study aims to answer the following questions:

  • What adverse events or medical complications occur following ONSS implantation and stimulation?
  • Does treatment with the ONSS reduce the frequency of cluster headache…

NCT07682090 — Transcutaneous Vagus Nerve Stimulation for Pain and Autonomic Dysfunction in Fibromyalgia (RESET-FMS)

StatusRecruiting
PhaseN/A
SponsorUniversity of Roma La Sapienza
Enrollment80
Study TypeINTERVENTIONAL
ConditionsFibromyalgia Syndrome
Interventions;

Fibromyalgia syndrome (FMS) is a chronic pain condition characterized by widespread pain, fatigue, sleep disturbances, cognitive symptoms, and autonomic dysfunction, significantly impairing quality of life. Increasing evidence suggests that, beyond central pain dysregulation, patients with FMS frequently exhibit autonomic nervous system dysfunction, characterized by sympathetic nervous system (…

NCT07604116 — A Study to Evaluate Satety, Tolerability, Biodistribution, Radiation Dosimetry, and Pharmacokinetics of SST001 in Healthy Volunteers, Patients With PD and Patients With MSA

StatusRecruiting
PhasePhase 1
SponsorSynusight Biotech (Shanghai) Co., Ltd.
Enrollment30
Study TypeINTERVENTIONAL
ConditionsMultiple System Atrophy (MSA); Parkinson’s Disease (PD)
Interventions

The non-randomized, open-label phase I study aims to evaluate the safety, tolerability, biodistribution, radiation dosimetry, and pharmacokinetics of SST001 in healthy volunteers, patients with MSA and patients with PD.

Active, Not Recruiting

NCT02994719 — Gait Analysis in Neurological Disease

StatusActive, not recruiting
PhaseN/A
SponsorBeth Israel Deaconess Medical Center
Enrollment120
Study TypeOBSERVATIONAL
ConditionsParkinson’s Disease; Parkinsonian Disorders; Atypical Parkinson Disease; Progressive Supranuclear Palsy; Multiple System Atrophy
Interventions;

The purpose of this study is to investigate whether speed-dependent measures of gait (so called gait signatures) can be identified in patients with neurological conditions that affect gait, particularly in subjects with parkinsonian disorders.

NCT03648905 — Clinical Laboratory Evaluation of Chronic Autonomic Failure

StatusActive, not recruiting
PhaseN/A
SponsorNational Institute of Neurological Disorders and Stroke (NINDS)
Enrollment89
Study TypeOBSERVATIONAL
ConditionsParkinson’s Disease; Multiple System Atrophy; Autonomic Failure
Interventions; ;

Background:

The autonomic nervous system controls automatic body functions. Researchers want to improve the tests used to diagnose autonomic failure. Orthostatic hypertension is a drop in blood pressure when a person stands up. Researchers want to focus on this sign of autonomic failure.

Objective:

To improve testing for conditions that cause autonomic nervous system failure.

Eligibility:

NCT05913687 — Automated Imaging Differentiation of Parkinsonism

StatusActive, not recruiting
PhaseN/A
SponsorUniversity of Florida
Enrollment315
Study TypeOBSERVATIONAL
ConditionsParkinson Disease; Multiple System Atrophy, Parkinson Variant; Progressive Supranuclear Palsy
Interventions

The purpose of this study is to test the performance of the AID-P across 21 sites in the Parkinson Study Group. Each site will perform imaging, clinical scales, diagnosis, and will upload the data to the web-based software tool. The clinical diagnosis will be blinded to the diagnostic algorithm and the imaging diagnosis will be compared to the movement disorders trained neurologist diagnosis.

NCT05664646 — Autonomic Effects of Stimulation in SCI

StatusActive, not recruiting
PhaseN/A
SponsorVA Office of Research and Development
Enrollment20
Study TypeINTERVENTIONAL
ConditionsSpinal Cord Injury
Interventions

This study aims to determine the effects of transcutaneous spinal cord stimulation to increase blood pressure and use that device to increase power output and heart rate recovery during arm cycle ergometry. In addition, the investigators will see if the stimulation helps regulate body temperature when in a cool environment.

NCT05923866 — A Phase 2 Study of ONO-2808 in Patients With Multiple System Atrophy

StatusActive, not recruiting
PhasePhase 2
SponsorOno Pharmaceutical Co., Ltd.
Enrollment92
Study TypeINTERVENTIONAL
ConditionsMultiple System Atrophy (MSA)
Interventions;

This is a Phase 2, double-blind, parallel-group, placebo-controlled study to assess the safety, tolerability, pharmacokinetics, pharmacodynamics, and efficacy of multiple doses of ONO-2808 in patients with MSA. This is the first study of ONO-2808 in patients with MSA.

NCT06188663 — SalT Supplementation in Older Adults With Orthostatic Intolerance Disorders

StatusActive, not recruiting
PhasePhase 2
SponsorUniversity of Galway
Enrollment42
Study TypeINTERVENTIONAL
ConditionsOrthostatic Hypotension
Interventions

Background

Orthostatic hypotension (OH) is a common cause of falls, and key source of morbidity and mortality due to injury (e.g. hip fracture). Current guidelines recommend increasing salt intake in patients with symptomatic orthostatic hypotension. However, the evidence underpinning this recommendation is poor, based primarily on small trials with very short-term follow-up (< 6 weeks).

Cli…

NCT07030218 — A Warning Red Flag Classification System to Predict Risk of Vasovagal Event During Office Hysteroscopy

StatusActive, not recruiting
PhaseN/A
SponsorTanvir Hospital
Enrollment100
Study TypeOBSERVATIONAL
ConditionsVasovagal Syncope (VVS); Presyncope
Interventions

The goal of this pilot cross sectional study is to identify participants at risk of vasovagal reaction/syncope(VVR/VVS) during office hysteroscopy. A predictive red flag classification system is being studied to improve procedural safety during office hysteroscopy. Researchers will perform office hysteroscopy as per the standard protocol by vaginoscopic technique. A nurse positioned at the head…

NCT07292090 — Yogabased Movements for Primary Headaches (Migraine and/or Cluster Headache) - YOURHEAD - a Pilot Study

StatusActive, not recruiting
PhaseN/A
SponsorKarolinska Institutet
Enrollment20
Study TypeINTERVENTIONAL
ConditionsCluster Headache - Episodic and Chronic; Migraine Headache; Migraine Headache, With or Without Aura; Migraine in Adults; Migraine Headaches
Interventions

Migraine and/or Cluster Headache: Study Overview

**Background:** Migraine and cluster headache are two primary headache disorders that significantly impact quality of life and functionality in those affected. According to the WHO’s recurring burden of disease reports, migraine is among the neurological conditions responsible for the highest number of years lost due to illness. The headache…

NCT07657520 — High-Altitude Neurodegeneration Cohort (HANC) Study

StatusActive, not recruiting
PhaseN/A
SponsorWest China Hospital
Enrollment20000
Study TypeOBSERVATIONAL
ConditionsMultiple System Atrophy
Interventions

Chronic physiological hypoxia has been implicated in the pathogenesis of multiple system atrophy (MSA), a fatal neurodegenerative disorder of unknown etiology. This prospective, multicenter, observational cohort study (Phase II of the High-Altitude Neurodegeneration Cohort [HANC] study) aims to validate the association between chronic hypoxia exposure and incident MSA risk. A total of 20,000 …

Not Yet Recruiting

NCT07670806 — Effects of an Osteopathic Manual Therapy Protocol on Heart Rate Variability, Stress, and Anxiety in Young Adults

StatusNot yet recruiting
PhaseN/A
SponsorEscola Superior de Tecnologia da Saúde do Porto
Enrollment30
Study TypeINTERVENTIONAL
ConditionsStress; Anxiety
Interventions; ;

Anxiety is characterized by excessive worry and anticipation of future threats, often accompanied by physiological and behavioral manifestations. Anxiety disorders are among the most prevalent mental health conditions worldwide and represent a significant public health concern, particularly among young adults and university students, who frequently experience academic, social, and financial str…

NCT07657507 — Presentation of Young Adults With and Without Joint Hypermobility

StatusNot yet recruiting
PhaseN/A
SponsorClarkson University
Enrollment100
Study TypeOBSERVATIONAL
ConditionsHypermobile Ehlers-Danlos Syndrome; Postural Orthostatic Tachycardia Syndrome (POTS)

People with multiple hypermobile joints are diagnosed with Generalized Joint Hypermobility (GJH) when asymptomatic, or Hypermobile Ehlers-Danlos Syndrome (hEDS) and Hypermobility Spectrum Disorder (HSD) when symptomatic (hEDS/HSD, or ‘HSD’ here). GJH likely affects about 20% of the U.S. population, while HSD affects 0.5-3% of the US population. Although joint hypermobility is the most visible p…

StatusNot yet recruiting
PhaseN/A
SponsorRiphah International University
Enrollment99
Study TypeINTERVENTIONAL
ConditionsDiabetic Peripheral Neuropathy Type 2
Interventions;

This study will examine how two types of exercise programs affect nerve health in people with diabetic peripheral neuropathy. Diabetic peripheral neuropathy is a common complication of type 2 diabetes that can cause numbness, pain, balance problems, and reduced quality of life. Exercise is often recommended for people with diabetes, but it is not yet clear which types of exercise are most effec…

NCT07674511 — Impact of Transcutaneous Spinal Stimulation on Blood Pressure and Orthostasis in Spinal Cord Injury

StatusNot yet recruiting
PhaseN/A
SponsorKessler Foundation
Enrollment10
Study TypeINTERVENTIONAL
ConditionsSpinal Cord Injuries; Hypotension; Orthostatic Hypotension; Spinal Cord Diseases; Cardiovascular Diseases
Interventions;

The purpose of this study is to learn whether stimulation applied to the spinal cord through the skin (called transcutaneous spinal stimulation) can help control blood pressure in people with a spinal cord injury.

The main questions this study attempts to solve:

  1. What are the immediate effects of spinal cord transcutaneous stimulation on BP?
  2. Does stimulation produce lasting improvements …

Enrolling by Invitation

NCT06306157 — Low Dose Naltrexone Therapy for Complex Regional Pain Syndrome

StatusEnrolling by invitation
PhasePhase 4
SponsorHospital for Special Surgery, New York
Enrollment40
Study TypeINTERVENTIONAL
ConditionsComplex Regional Pain Syndrome; Chronic Pain; Causalgia; Complex Regional Pain Syndrome Type I; Complex Regional Pain Syndrome Type II
Interventions;

Complex Regional Pain Syndrome (CRPS) is a rare and often debilitating chronic pain condition whereby individuals may experience extreme sensitivity, discoloration, and swelling of the affected area – along with numerous other painful symptoms. There are currently a limited number of treatment options available to those suffering with the condition, with various treatments including nerve bloc…

NCT07566871 — Effect of Non-Invasive Vagus Nerve Stimulation in Burn Patients

StatusEnrolling by invitation
PhaseN/A
SponsorFenerbahce University
Enrollment60
Study TypeINTERVENTIONAL
ConditionsBurn Injury
Interventions;

This study will evaluate the effects of non-invasive vagus nerve stimulation (nVNS) in adults with burn injuries. Burn patients may experience anxiety, poor sleep quality, pain, itching, and changes in autonomic nervous system function during recovery.

Participants will be randomly assigned to one of two groups. The intervention group will receive conventional physiotherapy plus nVNS, and the …

NCT07566923 — Effects of Non-Invasive Vagus Nerve Stimulation in Adolescent Burn Patients

StatusEnrolling by invitation
PhaseN/A
SponsorFenerbahce University
Enrollment60
Study TypeINTERVENTIONAL
ConditionsBurn Injury
Interventions;

This study will evaluate the effects of non-invasive vagus nerve stimulation in adolescents aged 12 to 18 years who have burn injuries. The study will include patients who have completed the acute phase after burn injury and who have symptoms such as anxiety, sleep problems, pain, or itching.

Participants will be randomly assigned to one of two groups. One group will receive conventional physi…

Completed Trials

NCT00465790 — Research of Biomarkers in Parkinson Disease

StatusCompleted
PhaseN/A
SponsorInstitut National de la Santé Et de la Recherche Médicale, France
Enrollment219
Study TypeOBSERVATIONAL
ConditionsParkinson Disease; Multiple System Atrophy; Progressive Supranuclear Palsy; Huntington Disease; Dystonia

The main goal of the GENEPARK consortium is to employ innovative haemogenomic approaches to determine gene expression profiles specific for genetic and idiopathic Parkinson’s disease (PD) patients. These gene expression signatures will be utilised clinically as non-invasive diagnostic tests for PD. The sensitivity of the newly developed diagnostic test will be determined by extensive validation…

NCT03924414 — Trial of Parkinson’s And Zoledronic Acid

StatusCompleted
PhasePhase 4
SponsorCalifornia Pacific Medical Center Research Institute
Enrollment2721
Study TypeINTERVENTIONAL
ConditionsParkinson Disease; Osteoporosis; Parkinsonism; Parkinson’s Disease and Parkinsonism; Atypical Parkinsonism
Interventions;

This home-based study is a randomized (1:1) placebo-controlled trial of a single infusion of zoledronic acid-5 mg (ZA) for the prevention of fractures in men and women aged 60 years and older with Parkinson’s disease and parkinsonism with at least 2 years of follow-up. A total of 2650 participants will be enrolled and randomized in the United States. Participants, follow-up outcome assessors, a…

NCT07691112 — Prevalence of Chapman Reflex Points in Medical Students and Their Association With Visceral Symptoms

StatusCompleted
PhaseN/A
SponsorThe Touro College and University System
Enrollment101
Study TypeOBSERVATIONAL
ConditionsHealthy; Autonomic Nervous System Diseases; Lymphatic Diseases; Somatic Dysfunction; Chapman Reflex Points
Interventions

Chapman Reflex Points (CRPs) are small palpable nodules found within connective tissue that have traditionally been associated with dysfunction of internal organs and the autonomic nervous system. However, little is known about how commonly these findings occur in healthy individuals or whether they are associated with symptoms experienced by otherwise healthy people.

The purpose of this study…

NCT04913051 — Interest of Day Hospital Care for Patients With Chronic Regional Pain Syndrome Referred to the Chronic Pain Unit for the First Time

StatusCompleted
PhaseN/A
SponsorCentre Hospitalier le Mans
Enrollment36
Study TypeOBSERVATIONAL
ConditionsChronic Regional Pain Syndrome

Chronic Regional Pain Syndrome (CRPS) is a chronic disabling disease. Patients present a variable picture associating pain localized to an articular or peri-articular region, motor and vasomotor disorders and trophic disorders.

Its pathophysiology, still poorly understood to this day, results from local inflammatory phenomena complicated by peripheral sensitization and central spinal and cereb…

NCT05807373 — Differential Diagnosis Between Parkinson’s Disease and Multiple System Atrophy Using Digital Speech Analysis - Part 2

StatusCompleted
PhaseN/A
SponsorUniversity Hospital, Bordeaux
Enrollment28
Study TypeINTERVENTIONAL
ConditionsParkinson Disease; Multiple System Atrophy
Interventions

Parkinson’s disease (PD) is the second most common neurodegenerative disease. Multiple system atrophy (MSA) is a relentlessly progressing rare neurodegenerative disease of unknown etiology. The differential diagnosis between the MSA-Parkinsonism (MSA-P) subtype and PD can be very challenging in early disease stages, while early diagnostic certitude is important for the patient because of the di…

NCT07005947 — Long COVID-19 Cutaneous Signatures: An ARPA Funded Research Project

StatusCompleted
PhaseN/A
SponsorCND Life Sciences
Enrollment237
Study TypeOBSERVATIONAL
ConditionsLong COVID-19; Acute COVID-19; Postural Orthostatic Tachycardia Syndrome (POTS); Diabetic Neuropathy

This is a prospective, longitudinal study involving 300 participants for a single visit to compare Long COVID-19 neurocutaneous biosignatures with those of other disorders affecting the sensory and autonomic nervous system.

NCT06968026 — Right Prefrontal Autonomic Mapping in Recurrent Pregnancy Loss With Comorbid Anxiety

StatusCompleted
PhaseN/A
SponsorShenyang Jinghua Hospital
Enrollment55
Study TypeINTERVENTIONAL
ConditionsRecurrent Pregnancy Loss; Anxiety Disorders
Interventions

Recurrent pregnancy loss is often accompanied by substantial anxiety and may also be associated with autonomic imbalance and increased long-term cardiovascular vulnerability. The present proof-of-concept rTMS-ECG parameter-finding trial will examine whether high-intensity, low-frequency, periodic repetitive transcranial magnetic stimulation (rTMS) delivered over the right dorsolateral prefronta…

NCT07045818 — Altered Interhemispheric DLPFC Coordination and Cardiac Hyperreactivity During Multisensory Aversive Challenge in Recurrent Pregnancy Loss With Comorbid Anxiety

StatusCompleted
PhaseN/A
SponsorShenyang Medical College
Enrollment70
Study TypeOBSERVATIONAL
ConditionsRecurrent Pregnancy Loss Without Current Pregnancy; Anxiety Disorder
Interventions

This exploratory clinical study, NEURO-CARD-2, will use simultaneous functional near-infrared spectroscopy (fNIRS) and electrocardiography (ECG) to investigate interhemispheric dysfunction in the dorsolateral prefrontal cortex (DLPFC) and its association with autonomic sympathetic activation in women with recurrent pregnancy loss (RPL) and comorbid anxiety. Using a standardized multisensory ave…

NCT07608887 — Effect of Hot Spring Therapy on Autonomic Nervous System and Exercise Performance During Altitude Training

StatusCompleted
PhaseN/A
SponsorMacao Polytechnic University
Enrollment27
Study TypeINTERVENTIONAL
ConditionsAltitude Training Adaptation; Autonomic Nervous System; Hydrotherapy; Exercise Performance; Altitude Sickness
Interventions; ;

This randomized controlled trial aims to investigate the effects of balneotherapy (hot spring bathing) on cardiac autonomic nervous system function and exercise performance in healthy athletes undergoing high-altitude training. Participants will be randomly assigned to the intervention group (receiving hot spring baths three times per week (38°C, 20 minutes) combined with high-altitude training…