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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03052595
Other study ID # APVV 15-0228
Secondary ID
Status Completed
Phase
First received
Last updated
Start date February 1, 2017
Est. completion date March 31, 2023

Study information

Verified date April 2023
Source Slovak Academy of Sciences
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Multiple sclerosis (MS) is a chronic inflammatory demyelinating disease of the central nervous system (CNS) and is one of the most common neurological diseases, often leading to disability of the patients. The MS pathogenesis includes vascular and inflammatory components, however recently also the role of mitochondrial dysfunction being a hot topic in neurodegeneration.


Description:

Multiple sclerosis (MS) is a chronic inflammatory demyelinating disease of the central nervous system (CNS) and is one of the most common neurological diseases, often leading to disability of the patients. The MS pathogenesis includes vascular and inflammatory components, however recently also the role of mitochondrial dysfunction being a hot topic in neurodegeneration. Current project is based on previous project results, where the investigators of this project found signs of insulin resistance (IR) with hyperinsulinemia in patients with MS, which seem not to be related to chronic inflammation or low physical activity. Therefore aim of the present project is to elucidate impact of mitochondrial dysfunction in the pathogenesis of impaired insulin action and its role in the neurodegenerative process. To test the hypothesis, mitochondrial function, endothelial function, changes in membrane proteins and function of autonomic nervous system will be assessed. Those parameters will be measured non-invasively and in samples of blood, cerebrospinal fluid and skeletal muscle. MS patients will be examined at the time of diagnosis and after 12 months of treatment; healthy subjects will be used as controls. Elucidation of insulin resistance cause and the role of mitochondrial dysfunction in pathogenesis of disease is expected. Potential outcome of the project could be the answer, if pharmacological or non-pharmacological intervention might lead to improvement of mitochondrial function and therefore represent a new approach to prevent MS progression.


Recruitment information / eligibility

Status Completed
Enrollment 70
Est. completion date March 31, 2023
Est. primary completion date March 31, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 45 Years
Eligibility Inclusion Criteria for MS patients: - Age: 18-45 years - Recent diagnosis of MS based on McDonald criteria - Functional disability defined by the EDDS in the range of 2 to 6 - Patient demonstrates ability to successfully perform physical therapy exercises and procedures independently or with assistance of a caregiver Exclusion Criteria: - smoking, pregnancy, lactation, received a course of steroids (intravenous or oral) within 60 days of screening, diabetes, hypertension

Study Design


Related Conditions & MeSH terms


Intervention

Diagnostic Test:
Oral glucose tolerance test
Oral glucose tolerance test to measure glucose and insulin concentrations after oral glucose load
Testing of autonomous nervous system function
Autonomous nervous system function will be assessed using a battery of tests (orthostasis, Valsalva manoeuvre, heart rate variability recording, blood hormone levels, ect.)
Stroop test
Stroop test will be used to test cognitive function

Locations

Country Name City State
Slovakia Biomedical Center, Slovak Academy of Sciences, Institute of clinical and translational reasearch Bratislava

Sponsors (2)

Lead Sponsor Collaborator
Slovak Academy of Sciences Comenius University

Country where clinical trial is conducted

Slovakia, 

Outcome

Type Measure Description Time frame Safety issue
Primary Insulin sensitivity Insulin sensitivity indices calculated from plasma glucose and insulin concentrations during oral glucose tolerance test 2017-2019
Secondary Expanded Disability Status Scale (EDSS) Expanded Disability Status Scale (EDSS) was developed for rating overall disability in MS. Patients are graded on the basis of presenting symptoms in eight different functional systems (FS), including pyramidal, cerebellar, brainstem, sensory, bowel and bladder, visual, mental, and other functions. Scoring of the EDSS uses a 0 to 10, 20-step scale, with 0 equal to normal neurological function, 6.0 requires an assistive device for walking and 10.0 equal to death due to MS. The final score is based on grades obtained in the FS assessment. 2017-2020
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