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Motor Neuron Disease clinical trials

View clinical trials related to Motor Neuron Disease.

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NCT ID: NCT03984708 Active, not recruiting - Clinical trials for Amyotrophic Lateral Sclerosis

New Therapeutic Strategy in ALS Based on Metabolic Status and Associated Metabolic Pathways.

METABOCALS
Start date: January 27, 2020
Phase: N/A
Study type: Interventional

Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease that affects central and peripheral motor neurons. None of the clinical trials conducted have been clearly successful and the disease remains incurable, putting patients' vital prognosis at risk in the medium term. An alteration of the basal metabolism leading to hypermetabolism has been described in several articles in the literature. The causes of this hypermetabolism and the precise exploration of the metabolic pathways involved are still poorly understood. The fibroblasts of ALS patients may be the site of some metabolic disturbances in this disease with a hypothetical specific basal metabolic profile. These cells are adapted to different metabolic explorations such as omnic approaches. Superficial skin biopsy followed by fibroblast culture can provide a considerable biobank. This cellular richness will allow us, in ALS patients and their controls, to perform metabolomic and lipidomic approaches, as well as the quantification transcriptomic approach."

NCT ID: NCT03981536 Active, not recruiting - Clinical trials for Amyotrophic Lateral Sclerosis

A Study to Evaluate AP-101 in Familial and Sporadic Amyotrophic Lateral Sclerosis (ALS)

Start date: October 10, 2019
Phase: Phase 1
Study type: Interventional

Single ascending doses of AP-101 will be administered by intravenous (IV) infusion

NCT ID: NCT03912987 Active, not recruiting - Clinical trials for Amyotrophic Lateral Sclerosis

TRIAL READY (Clinical Trial Readiness)

Start date: January 22, 2019
Phase:
Study type: Observational

This study, being conducted under the auspice of the CReATe Consortium, will enroll patients with ALS and related disorders as well as healthy controls, with the goal of facilitating clinical validation of leading biological-fluid based biomarker candidates that may aid therapy development for patients with ALS and related disorders.

NCT ID: NCT03811301 Active, not recruiting - Clinical trials for Spinal Cord Injuries

[BrainConnexion] - Neurodevice Phase I Trial

Start date: November 21, 2017
Phase: N/A
Study type: Interventional

This study aims to evaluate the safety of a wireless implantable neurodevice microsystem in tetraplegic patients, as well as the efficacy of the electrodes for long-term recording of neural activities and the successful control of an external device.

NCT ID: NCT03800524 Active, not recruiting - Clinical trials for Amyotrophic Lateral Sclerosis (ALS)

Safety and Efficacy of TUDCA as add-on Treatment in Patients Affected by ALS

TUDCA-ALS
Start date: February 22, 2019
Phase: Phase 3
Study type: Interventional

This is a Phase III, multi-centre, randomized, double-blind, placebo-controlled, parallel-group study to evaluate Safety and Efficacy of Tauroursodeoxycholic (TUDCA) as add-on Treatment in Patients Affected by Amyotrophic Lateral Sclerosis (ALS).

NCT ID: NCT03766321 Active, not recruiting - Clinical trials for Amyotrophic Lateral Sclerosis

Fecal Microbiota Transplantation Effect on Amyotrophic Lateral Sclerosis Patients

FETR-ALS
Start date: July 1, 2020
Phase: N/A
Study type: Interventional

Given the role of adaptive immunity in ALS, the pathogenicity of some clostridial strains on motorneurons, the putative role of cyanobacteria in ALS development, and the increasing interest for microbiota in neurodegenerative disorders, the modification of intestinal microbiota might affect ALS at its core. This interventional study aims at evaluating the biological and disease-modifying effects of Fecal Microbiota Transplant (FMT) in patients affected by Amyotrophic Lateral Sclerosis. As a primary aim of the study, the investigators postulate ALS patients treated with FMT compared to the control arm will display increased Tregs number, which is a favourable biomarker of disease activity and progression. Clinical outcomes as disease progression measured by ALS Functional Rating Scale Revised (ALSFRS-R) score, survival, respiratory function and quality of life will be assessed during the whole treatment and follow-up period. Moreover, biological activity of FMT will be evaluated in different biomatrices, together with FMT safety and tolerability in a cohort of ALS patients.

NCT ID: NCT03764384 Active, not recruiting - Clinical trials for Amyotrophic Lateral Sclerosis

Validation Of Tidal/End -Tidal CO2 in ALS

VOTECO2ALS
Start date: August 20, 2018
Phase:
Study type: Observational

The study team propose that a new, hand-held test device may be valuable in the management of breathing failure in patients with Motor Neurone Disease (MND). The study team need to validate this device against the current gold standard of blood gas analysis and determine whether people with MND can use it at home. The new device, called 'N-Tidal C™' measures the carbon dioxide (CO2) in expired breath. At the end of the breath (end tidal) the CO2 level gives an indication of the CO2 in the person's arterial blood. Ventilatory failure is diagnosed at present using the value of CO2 in the arterial blood, but usually this can only be measured in specialist clinics. The study will determine if the end tidal CO2 measured by the new device agrees with CO2 measured on a blood test in clinic and also whether or not the device is practical for home use. The team will analyse the output of the device during home monitoring to see if changes in the pattern of CO2 in the expired breath identify, or even predict, the development of breathing failure in the community. With the results of these measures and detailed information about the patients in Papworth's clinic, recruited to this study, collected over a year the team will design a follow on study to see if using the new device at home can improve survival and quality of life for people with MND.

NCT ID: NCT03690791 Active, not recruiting - Clinical trials for Amyotrophic Lateral Sclerosis

Efficacy of Cannabinoids in Amyotrophic Lateral Sclerosis or Motor Neurone Disease

Start date: January 9, 2019
Phase: Phase 3
Study type: Interventional

This is a randomised, double-blind, placebo controlled study on a cannabis-based medicine extract (MediCabilis CBD Oil), in patients with Amyotrophic Lateral Sclerosis or Motor Neurone Disease. Participants will be randomised in a 1:1 ratio to receive MediCabilis CBD Oil or placebo oil. The treatment duration is 6 months with one-month safety follow up. Participants will be checked every month either face to face or via telephone and will be assessed to collect data for study objectives such as ALSFRS-R, Forced Vital Capacity, pain and spasticity score, and quality of life. Thirty (30) participants will be randomised.

NCT ID: NCT03651349 Active, not recruiting - Clinical trials for Amyotrophic Lateral Sclerosis

To Determine the Maximum Tolerated Dose (MTD) of HK-001 in Healthy Volunteers

Start date: February 1, 2021
Phase: Phase 1
Study type: Interventional

Eligible subjects will receive either different dosages of HK-001 or placebo in a 3:1 ratio in 1 of the 7 dose cohorts. After single dose administration, followed by an independent Data and Safety Monitoring Board (DSMB) meeting for safety assessments (including the available plasma pharmacokinetic profile), the subjects will be allowed to receive (Z)-BP or placebo twice a day orally at the study site for 14 consecutive days and follow up on the 28th day after the last dose administration by a site visit. The study drugs (including placebo) will be administered at the study site by following the investigator's instructions to either perform blood sampling for pharmacokinetic evaluation or maximize the treatment compliance. There will be 7 cohorts and subjects will be randomized into cohorts consisting of 8 subjects each (6 active and 2 placebo controls per cohort). Dose cohorts will be escalated sequentially from low to high dose (50 mg, BID; 100 mg, BID; 150 mg, BID; 225 mg, BID; 300 mg, BID; 400 mg, BID; 525 mg, BID) by following a modified Fibonacci sequence, and based on the decision of an independent DSMB at a set time point. Following all subjects of a cohort complete the safety and PK evaluation after receiving the last dose administration, a cohort at the next dose level will be launched if the DSMB does not identify significant safety concerns after reviewing safety data and PK profiles.

NCT ID: NCT03604822 Active, not recruiting - Dysphagia Clinical Trials

Music Therapy Protocol to Support Bulbar and Respiratory Functions in ALS

Start date: September 27, 2017
Phase: N/A
Study type: Interventional

This study evaluates potential of music therapy treatment to support breathing, speech, swallow and cough of persons with amyotrophic lateral sclerosis (ALS). Music therapy is the clinical use of music and its elements to enhance human health and wellbeing. Application of music therapy principles in neurorehabilitation allow to treat cognitive, sensory, and motor dysfunctions.