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Sclerosis clinical trials

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NCT ID: NCT05688436 Recruiting - Multiple Sclerosis Clinical Trials

A Study to Assess Pregnancy Outcomes in Women Exposed to Diroximel Fumarate

Start date: September 24, 2021
Phase:
Study type: Observational [Patient Registry]

The primary objective of the study is to estimate the prevalence of major congenital malformations (MCMs) and compare the prevalence between the diroximel fumarate (DRF) and comparator groups. The secondary objectives of the study are to estimate the incidence of spontaneous abortion (SA) and compare the incidence between the DRF and comparator groups; to estimate the incidence of preterm birth and compare the incidence between the DRF and comparator groups; to estimate the incidence of stillbirth and compare the incidence between the DRF and comparator groups and to estimate the prevalence of small for gestational age (SGA) and compare the prevalence between the DRF and comparator groups.

NCT ID: NCT05685784 Recruiting - Clinical trials for Progressive Multiple Sclerosis

Multiple Sclerosis Prediction and Monitoring of Progression Study

PREMONITION
Start date: March 1, 2022
Phase: N/A
Study type: Interventional

Multiple sclerosis (MS) is a auto-immune disease that is mostly characterized by acute clinical relapses and/or focal inflammation in the central nervous system (CNS) followed by recovery. Yet, a significant part of the patients also experience a progressive decline in function. This progressive phase usually has an insidious onset causing a delay for diagnosis and adjusted therapies. There are plenty of clinical assessments available to measure walking speed, cognition, sleep,.... . But these assessments are merely a snapshot of the patient 's symptoms. By monitoring these parameters at home, real life data can be provided to capture subclinical signs of progression. The goal of this study is to detect a digital biomarker for progressive MS at an earlier stage next to validating wearables by comparing them to golden standard measurements such a polysomnography or gait analysis in a specialized lab.

NCT ID: NCT05676099 Recruiting - Tuberous Sclerosis Clinical Trials

TSC Biosample Repository and Natural History Database

Start date: January 2016
Phase:
Study type: Observational [Patient Registry]

The TSC Biosample Repository collects and stores samples of blood, DNA, and tissues that scientists can request to use in their research. The samples we collect are all linked to clinical data in the TSC Natural History Database. The TSC Natural History Database captures clinical data to document the impact of the disease on a person's health over his or her lifetime. This data may be collected retrospectively or prospectively.

NCT ID: NCT05671588 Recruiting - Multiple Sclerosis Clinical Trials

Cardiovascular Fitness of Patients With Multiple Sclerosis, Effect of Exercise on Fatigue and Depression

Start date: May 1, 2022
Phase: N/A
Study type: Interventional

This study is focused on patients with multiple sclerosis (MS), their cardiovascular fitness, and the effect of combined controlled training on the perception of fatigue, the development of depression, and quality of life in the first year after diagnosis.

NCT ID: NCT05661266 Recruiting - Multiple Sclerosis Clinical Trials

Investigating Eye-Movement Biomarkers of Disease Severity and Cognition in Multiple Sclerosis

Start date: August 16, 2023
Phase:
Study type: Observational [Patient Registry]

The overarching goal of this research protocol is to acquire eye-tracking, cognitive, and disease-severity metrics in multiple sclerosis (MS) patients to further build up a database of MS patients and train a machine learning classifying algorithms to identify which eye-tracking metrics-or combination thereof-can serve as reliable markers of MS disease severity and cognitive status.

NCT ID: NCT05660187 Recruiting - Multiple Sclerosis Clinical Trials

VIRtual Versus UsuAL In-office Care for Multiple Sclerosis (VIRTUAL-MS)

VIRTUAL-MS
Start date: March 31, 2023
Phase: N/A
Study type: Interventional

The current standard of outpatient MS care depends on in-clinic visits, but MS patients face many barriers to accessing this care. These barriers include those resulting from the disease itself, such as physical limitations, driving restrictions and financial limitations, and they are further compounded by an overall shortage of neurologists. Furthermore, MS care has a significant economic impact, with the estimated indirect and direct costs for treating MS in the US estimated to be > $85.4 billion. Therefore, there is a need to improve access to and reduce cost of MS care, and telehealth is a potential solution. The VIRTUAL-MS study has been designed to evaluate the impact of telehealth care on MS clinical outcomes, costs, and satisfaction compared to in-person care. Additionally, the study aims to evaluate facilitators and barriers to telehealth use to inform widespread implementation.

NCT ID: NCT05658601 Recruiting - Clinical trials for Multiple Sclerosis, Relapsing-Remitting

A Study to Describe the Switching From a First- or Second-line Disease Modifying Therapy (DMT) to Ozanimod in Participants With Relapsing Remitting Multiple Sclerosis (RRMS)

SWITCH - ITA
Start date: July 14, 2023
Phase:
Study type: Observational

The purpose of this study is to describe the reasons, therapy, and/or disease for changing first or second line Disease Modifying Therapy (DMT) to ozanimod in participants with Relapsing Remitting Multiple Sclerosis (RRMS).

NCT ID: NCT05648292 Recruiting - Clinical trials for Multiple Sclerosis, Relapsing-Remitting

The Relationships Between Personal Identity, Autobiographical Memory and Future Thinking in People With Multiple Sclerosis

SELFSEP
Start date: December 7, 2022
Phase:
Study type: Observational [Patient Registry]

Personal identity is composed of multiple facets of the self that are constructed and nourished through memories of past experiences (i.e., autobiographical memory) and the imagination of events that may occur in the future (i.e., future thinking) . While our previous work has shown that people with relapsing-remitting multiple sclerosis (pwRRMS) have autobiographical memory and future thought disorders, their impact on personal identity has not yet been explored. Based on a cognitive and clinical neuropsychology approach, this research project aims to better understand the cognitive mechanisms involved in the relationship between identity, autobiographical memory and future thinking in pwRRMS. We will examine the extent to which pwRRMS manage to maintain and reshape their identity through life experiences, with a particular interest in the potential integration of the disease as a facet of their identity. In addition, we will explore the positive and/or negative consequences of disease-related identity changes on emotional well-being and quality of life, as well as their links with the duration and severity of the disease. Overall, this research project will contribute to identify new therapeutic levers that can be used for the development of adapted and personalized care.

NCT ID: NCT05634993 Recruiting - Multiple Sclerosis Clinical Trials

Disability Level and Trunk Control in Individuals With Multiple Sclerosis

Start date: June 1, 2022
Phase:
Study type: Observational

Trunk control disorders are frequently encountered in individuals with MS. Trunk control is very important for safe and quality movement. Impairment of trunk control reduces the level of independence of individuals during activities of daily living. For this reason, it is extremely important to evaluate the trunk in the examination and treatment of individuals. When the literature was examined, it was seen that studies examining trunk control were insufficient. Therefore, our study was planned to investigate the relationship between disability level and trunk control in individuals with MS.

NCT ID: NCT05634967 Recruiting - Multiple Sclerosis Clinical Trials

Kesimpta (Ofatumumab) Pregnancy Registry

Start date: January 5, 2023
Phase:
Study type: Observational

The Kesimpta Pregnancy Registry is an observational, exposure cohort designed study to examine pregnancy and infant outcomes in women and infants who are exposed to Kesimpta (ofatumumab) during pregnancy to treat MS.