A Pilot Study to Investigate Glymphatic System Alterations in Vivo in Patients With Clinically Isolated Syndrome, Using Magnetic Resonance Imaging

Status: Recruiting
Location: See all (2) locations...
Intervention Type: Other
Study Type: Observational
SUMMARY

The brain possesses a system to get rid of unwanted substances, named Glymphatic System (GS). When this system is faulty, these accumulate, there is local inflammation, and progressive death of the cells. This occurs in neurological diseases including Parkinson's, or Alzheimer's. Inflammation and progressive death of the cells are also present in another neurological disorder, named Multiple Sclerosis (MS). Doctors think that GS dysfunction plays a role in MS too. In this research therefore, the aim is to study whether it drives inflammation, and disease progression in MS patients. The researchers have developed a new way to find signs of alteration of the GS using a scan named Magnetic Resonance Imaging (MRI) and will use it in a pilot study on patients with a condition named Clinically Isolated Syndrome (CIS), which often represents the very beginning of MS. It would therefore be demonstrated that the GS is a new mechanism of disease in CIS, which may associate with the symptoms, or the alterations in the levels of some substances in the blood suggestive of brain cells damage. Should this study be successful, this would provide preliminary evidence to perform a larger research study to assess if GS dysfunction drives the progression of MS.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: t
View:

• Male or female, aged 18 or over

• Suitable physically and psychologically to undertake the assessments, as judged by the Investigator

• Have voluntarily provided informed consent and have signed an ICF indicating that the purpose of the study has been explained and are willing and able to adhere to the study procedures described in the ICF.

• (For CIS group): A diagnosis of CIS or MS at first presentation

• Subjects must not have taken corticosteroids or IVIg or plasma-exchange within the 30 days prior to consent

• Adequate vision and hearing to perform the study procedures

• Medically healthy with no clinically significant findings on physical examination, laboratory profiles, vital signs at screening (with the exception of the signs of the condition under investigation)

• Women of child-bearing potential must practice a medically acceptable method of birth control. Acceptable methods include oral contraceptive, contraceptive patch, long-acting injectable contraceptive, or double-barrier method (condom or intrauterine device with spermicide).

• If on immunomodulatory medication, patients must have started it at least 30 days from screening and should not change their medication dose for the duration of the study.

Locations
Other Locations
United Kingdom
Royal Devon University Healthcare NHS Foundation Trust
RECRUITING
Exeter
University of Exeter
NOT_YET_RECRUITING
Exeter
Contact Information
Primary
Edoardo R de Natale, MD
e.de-natale@exeter.ac.uk
07503741242
Backup
Holly Wright
h.wright3@exeter.ac.uk
Time Frame
Start Date: 2024-05-01
Estimated Completion Date: 2025-12-31
Participants
Target number of participants: 30
Treatments
Clinically Isolated Syndrome
Patients with a diagnosis of Clinically Isolated Syndrome
Healthy Controls
Age- and gender-matched healthy controls.
Related Therapeutic Areas
Sponsors
Leads: University of Exeter

This content was sourced from clinicaltrials.gov