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Search / Trial NCT01667497

Does Fampridine SR Improve Cognitive Fatigue in Multiple Sclerosis Patients?

Launched by LONDON HEALTH SCIENCES CENTRE · Aug 16, 2012

Trial Information

Current as of August 02, 2025

Completed

Keywords

Cognitive Fatigue Multiple Sclerosis

ClinConnect Summary

Fampridine-SR (4-aminopyridine) is a slow release oral medication that acts as a selective neuronal potassium-channel blocker. It has been investigated in several multiple sclerosis (MS) studies and has been shown to improve ambulation, fatigue, and endurance. The hypothesis for the mode of action of fampridine in MS patients is based on the fact that demyelinated axons do not effectively conduct action potentials partly due to abnormal potassium currents that contribute to conduction failure by decreasing action potential duration and amplitude. Thus, potassium channel blockers such as 4-a...

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • Males/Females who are ≥ 18 years old and \< 65 years old
  • Capable of understanding and complying with the protocol, including speaking and writing fluent English and having at least a 9th grade education
  • Have a diagnosis of Relapsing Remitting, Secondary Progressive or Primary Progressive MS, as per revised McDonald's Criteria
  • Have not received steroids in last thirty (30) days or a relapse in the last sixty (60) days, and whose MS is considered stable
  • Have a PASAT CF z-score that is worse than 1.5 SD below the mean (\<-1.5 SD).
  • Have an Expanded Disability Status Scale (EDSS) of ≤ 7.0
  • Have given written informed consent prior to any study-related procedure not part of normal medical care, with the understanding that consent may be withdrawn by the subject at any time without prejudice to his/her future medical care
  • Are capable of performing the requirements of a NP test battery including at least 20/70 near visual acuity by near vision chart, with correction allowed
  • If female, must neither be pregnant nor breast-feeding
  • Exclusion Criteria:
  • Have cognitive deficits caused by concomitant medication usage or other significant neurological/psychological disease e.g. Alzheimer's disease, Parkinson's disease, stroke, transient ischemic attack, Vascular Dementia, Huntington's disease, traumatic brain injury or chronic CNS infection
  • Have evidence of other medical cause(s) of cognitive impairment
  • Have evidence of major depression as determined by a positive BDIFS and clinician interview
  • Have a history of uncontrolled hypertension, tachycardia or cardiovascular or disease
  • Have a history or current presentation of seizure
  • Are currently taking compounded 4-aminopyridine or another form of fampridine
  • Have a known hypersensitivity to any medical or non-medical ingredient of the medication tablet.
  • Have evidence of renal impairment (creatinine clearance ≤ 80 mL/min)
  • Are taking medications that are inhibitors of the renal organic cation transporter 2 (OCT2)
  • Have a diagnosis of colour blindness

About London Health Sciences Centre

London Health Sciences Centre (LHSC) is a leading academic health organization in Canada, dedicated to advancing healthcare through innovative research, education, and clinical excellence. As a prominent sponsor of clinical trials, LHSC leverages its state-of-the-art facilities and multidisciplinary expertise to facilitate groundbreaking research that aims to improve patient outcomes and enhance treatment options. The Centre collaborates with various stakeholders, including researchers, healthcare professionals, and industry partners, to ensure the highest standards of ethics and patient safety are upheld throughout the trial process. Through its commitment to scientific inquiry and evidence-based practice, LHSC plays a pivotal role in the evolution of modern medicine.

Locations

London, Ontario, Canada

Patients applied

0 patients applied

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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