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Libyan Multiple Sclerosis Registry Study

Multiple Sclerosis Care in a Conflict-Affected Health System: Diagnostic Delay, Treatment Access, and Disability Outcomes in Libya

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07264725
Enrollment
369
Registered
2025-12-04
Start date
2023-08-02
Completion date
2025-04-30
Last updated
2025-12-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Multiple Sclerosis

Keywords

Multiple Sclerosis MS Relapsing-Remitting MS Secondary Progressive MS Primary Progressive MS

Brief summary

This study aims to understand differences in access to diagnosis and treatment for people with multiple sclerosis (MS) receiving care in Libya. The study uses data from the Libyan Multiple Sclerosis Registry, which collects clinical and treatment information from patients at two tertiary neurology centres. The main focus is to examine how long it takes for patients to receive an MS diagnosis, who has access to high-efficacy disease-modifying therapies, and how these factors relate to disability levels. The results will help identify gaps in MS care within a conflict-affected health system and guide improvements in services for patients in Libya.

Interventions

DRUGDisease-Modifying Therapies

This is an observational study. No medications are assigned, administered, or modified by the study team. Disease-modifying therapies (DMTs) are recorded only as exposure variables based on routine clinical care. All drugs listed in this record are prescribed independently by treating neurologists as part of standard care, and the study does not influence treatment decisions in any way.

Sponsors

University of Zintan
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

* Adults aged 18 years or older * Diagnosis of multiple sclerosis according to the 2017 McDonald criteria * Receiving care at Tripoli University Hospital or Omar Askar Hospital * Able to provide written informed consent * Recorded EDSS score at registry entry * Availability of core demographic and diagnostic information

Exclusion criteria

* Clinically isolated syndrome (CIS) * Age younger than 18 years * Absence of confirmed multiple sclerosis diagnosis * Missing key clinical variables required for primary analysis (EDSS, phenotype, or DMT information) * Declined or unable to provide informed consent

Design outcomes

Primary

MeasureTime frameDescription
Moderate-to-Severe Disability (EDSS ≥3.0)At registry entryDisability measured using the Expanded Disability Status Scale (EDSS). Moderate-to-severe disability is defined as EDSS ≥3.0, assessed by trained neurologists using standardised procedures.

Secondary

MeasureTime frameDescription
EDSS Ordinal Disability CategoriesAt registry entryDisability severity categorised using the Expanded Disability Status Scale (EDSS) into three groups: 0-2.5 (mild), 3.0-5.5 (moderate), and ≥6.0 (severe). EDSS scores are assessed by trained neurologists at the time of registry entry.

Countries

Libya

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026