Influence of Fampridine on Working Memory in Individuals With Post COVID-19 Condition With Subjective Cognitive Impairment

Working Memory Clinical Trial

— FamC  

Official title:

Randomized Placebo-controlled Phase II Cross-over Study on the Influence of Fampridine on Working Memory in Individuals With Post COVID-19 Condition With Subjective Cognitive Impairment

Clinical Trial Details — Status: Active, not recruiting

Administrative data

• NCT number: NCT05274477
• Other study ID #: 2022-00452
• Status: Active, not recruiting
• Phase: N/A
• Start date: June 28, 2022
• Est. completion date: June 30, 2024

Study information

• Verified date: May 2024
• Source: University of Basel
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

In genome-wide association studies we identified potassium channels to be genetically linked to performance and neural activity of working memory in healthy humans. Furthermore, there is evidence in rodents and non-human primates that pharmacological blockade of potassium channels can improve working memory. In the present study, we aim at investigating the effects of 10 mg fampridine (4-Aminopyridine), a potassium channel-blocking agent, on working memory performance in individuals with Post-COVID-19-Condition with subjective cognitive impairment. The hypothesis is that fampridine improves working memory performance. Fampridine, especially its slow-release formulation (Fampyra®) is generally a safe drug with well-studied pharmacokinetic properties. It crosses the blood-brain barrier and reaches maximum concentration in the brain approximately 3.5h after single-dose administration. Evidence suggests that fampridine improves walking speed in patients with multiple sclerosis (MS), which led to FDA and EMA approval for this indication. The mode of action by which fampridine improves walking speed is probably its blockade of a spectrum of potassium channels that are exposed in demyelinated axons, leading to mitigation of potassium leakage and normalization of nerve conduction. Additionally, an action of fampridine at central synapses and increase of neurotransmitter release has been discussed.

Recruitment information / eligibility

• Status: Active, not recruiting
• Enrollment: 44
• Est. completion date: June 30, 2024
• Est. primary completion date: June 30, 2024
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 69 Years

Eligibility

Inclusion Criteria:

• male or female;
• a valid positive PCR test or a documented certified rapid antigen test or a virus-specific antibody (nucleocapsid) test for COVID-19 issued at least 3 months prior to study;
• Above medium subjective working memory impairment (at least "much worse" in item 1a part 2 (cognitive abilities) of the Covid-Q screening questionnaire;
• present at least 3 months after COVID-19 infection and lasting for at least 2 months. (The impairment must have emerged after COVID-19 infection and cannot be explained by an alternative diagnosis);
• normotensive (BP: 90/60mmHg - 140/90mmHg);
• BMI: 19.0 - 40.0 kg/m2;
• Age: 18 - 69 years;
• fluent German-speaking;
• IC as documented by signature.

Exclusion Criteria:

• initiation of pharmacological treatment or change of dose within the 30 days preceding the present study
• contraindications to the class of drugs under study, e.g. known hypersensitivity or allergy to 4-aminopyridine
• use of potassium channel blockers within the last 3 months
• concomitant treatment with OCT 2 inhibitors and -substrates (e.g. cimetidine, propranolol)
• acute or chronic psychiatric disorder (e.g. major depression, psychosis, somatoform disorder, suicidal tendency)
• acute cerebrovascular condition
• history of seizures
• risk of lowered seizure threshold (due to e.g. sleep deprivation, withdrawal of alcohol after alcohol abuse)
• renal impairment
• history of malignant cancers
• walking problems (e.g. due to dizziness)
• other clinically significant concomitant disease states that could pose a safety risk (e.g. hepatic dysfunction, cardiovascular disease, urinary tract infection)
• bradycardia < 50/min during clinical examination
• clinically significant laboratory or ECG abnormality that could be a safety issue in the study
• known or suspected non-compliance (e.g. missing more than one dose of study medication per intervention phase)
• drug or alcohol abuse
• inability to follow the procedures of the study, e.g. due to language or psychological problems of the participant
• participation in another study with an investigational drug within the 30 days preceding and during the present study
• enrolment of the investigator, his/her family members, employees and other dependent persons
• pregnancy or breast feeding
• Intensive care treatment due to COVID-19 infection. Exclusion Criteria concerning TMS measurement
• metal in the brain, skull or elsewhere in the body (e.g., splinters, fragments, clips, etc.)
• implanted neurostimulator (e.g., DBS, epidural/subdural, VNS)
• cardiac pacemaker or intracardiac lines
• medication infusion device
• piercings in the head area, pivot teeth (retainers are no exclusion criterion)
• tattoos (in the head area) with metallic inks or newly stung tattoos (< 3 months), as newly stung tattoos can be damaged by a magnetic field;
• condition after neurosurgery
• hearing problems or tinnitus
• not able to sit still due to tremor, tics, itching
• History of repeated syncope
• head trauma diagnosed as concussion or associated with loss of consciousness
• diagnosis of epilepsy, or a convulsion or a seizure in the past of the participant or his family
• TMS in the past showing problems
• MRI in the past showing problems
• surgical procedures to spinal cord
• spinal or ventricular derivations TMS measurement is optional. If a participant is eligible for the study, but prefers not to undergo TMS measurement or meets one or more exclusion criteria for TMS measurement, the participant can nevertheless be included in the study without rMT measurement using TMS.

Related Conditions & MeSH terms

• Cognitive Dysfunction
• COVID-19
• Working Memory

Intervention

Drug:
• Fampridine SR
Fampridine SR is an inhibitor of voltage gated potassium channels and is approved in Switzerland for treatment of gait problems in patients with Multiple Sclerosis (MS).
• Placebo
no active component

Locations

Country	Name	City	State
Switzerland	University of Basel, Transfaculty Research Platform	Basel	BS

Sponsors (3)

Lead Sponsor	Collaborator
Prof. Dominique de Quervain, MD	Clinical Trial Unit, University Hospital Basel, Switzerland, University Hospital, Basel, Switzerland

Country where clinical trial is conducted

Switzerland, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Digits Span backward performance	The Digit Span task is a subtest of an intelligence test for adults ("Wechsler Intelligenztest für Erwachsene" (WIE; (von Aster 2006)). Total scores for digit span backward will be calculated as described in the manual of the WIE. Minimum 0 points and maximum 12 points. Parallel version will be used for the altogether four assessments at the beginning (visits 2 and 4) and at the end (visits 3 and 5) of both treatment phases.	first and last day of 3.5-days-treatment periods (each 4 hours after intake in the morning); to assess changes between the verum and placebo condition
Secondary	Digits Span forward performance	The Digit Span task is a subtest of an intelligence test for adults ("Wechsler Intelligenztest für Erwachsene" (WIE; (von Aster 2006)). Total scores for digit span backward will be calculated as described in the manual of the WIE. Minimum 0 points and maximum 12 points. Parallel version will be used for the altogether four assessments at the beginning (visits 2 and 4) and at the end (visits 3 and 5) of both treatment phases.	first and last day of 3.5-days-treatment periods (each 4 hours after intake in the morning); to assess changes between the verum and placebo condition
Secondary	Red Button Task	Reaction time test (Red Button Task), adapted from (Dinges and Powell, 1985): participant sits in front of a screen showing a gray circle in the middle of the screen. The circle's color turn into red and participant will be instructed to push a button as soon as the color changes. The period between the time of color change and button push is measured in miliseconds and will be considered as reaction time.	first and last day of 3.5-days-treatment periods (each 4 hours after intake in the morning); to assess changes between the verum and placebo condition
Secondary	Symbol Digit Modalities Test, SDMT	Symbol Digit Modalities Test, SDMT (Smith 2013, 13th edition), a processing speed test. The test consists of the presentation of a series of 9 symbols, each of them is paired with a single digit, labelled 1-9, in a key at the top of a sheet. The remainder of the page has a pseudorandomized sequence of the symbols and the participant must respond with the digit associated with each of these as quickly as possible. The score is the number of correct answers in 90 seconds. The administration of SDMT will be preceded by a learning sequence at both timepoints. It will be used parallel versions for all test days.	first and last day of 3.5-days-treatment periods (each 4 hours after intake in the morning); to assess changes between the verum and placebo condition
Secondary	Verbal episodic memory performance (word list)	Verbal episodic memory performance (15 words) measured by immediate and delayed word-list recall. Adapted from a subtest of the German test called "Verbaler Lern- und Merkfähigkeits-Test" (VLMT; Helmstaedter/Lendt/Lux, 2001).	first and last day of 3.5-days-treatment periods (each 4 hours after intake in the morning); to assess changes between the verum and placebo condition
Secondary	Lexical ability	Lexical ability measured by phonemic fluency test after acute and repeated intake of study medication (S-words); adapted from a subtest of the German test called "Regensburger Wortflüssigkeits-Test" (RWT; Aschenbrenner/Tucha/Lange, 2001). In this task participants should name orally as many words as possible initiating with a special letter in one minute (e.g. Mary, Milk, Mouse, etc. for the letter M) the number of unique meaningful words will be considered as the participant's score.	first and last day of 3.5-days-treatment periods (each 4 hours after intake in the morning); to assess changes between the verum and placebo condition
Secondary	Bochumer Matrizentest (BOMAT - standard)	Fluid intelligence (Gf) will be measured with the Bochumer Matrizentest (BOMAT - standard; Hossiep/Hasella, 2010, 1st edition), matrix reasoning. BOMAT - standard consisting of 30 items will be administred. Parallel version will be used for the altogether four assessments at the beginning (visits 2 and 4) and at the end (visits 3 and 5) of both treatment phases. To create four versions, the original BOMAT versions A and B have been divided each into two versions (every second item) with 15 items each. A time-limited version (10 minutes) will be used to avoid a ceiling effect. The total score is calculated by summing the correct solutions, ranging between 0 to 15.	first and last day of 3.5-days-treatment periods (each 4 hours after intake in the morning); to assess changes between the verum and placebo condition
Secondary	Subjective cognitive impairment	Subjective cognitive symptoms are assessed with a self-administered questionnaire at the end of both treatment phases (visits 3 and 5). The participants are asked to rate the changes of cognitive abilities during the three 3 days of the treatment phase as compared to the 3 days before treatment on a 7 point likert scale (much worse - (…) - unchanged - (…) much better).This questionnaire contains questions about several domains of cognitive function (working memory, episodic memory, attention and concentration, executive function, lexical ability).	during the three 3 days of the treatment phase as compared to the 3 days before treatment; to assess changes between the verum and placebo condition
Secondary	Resting motor threshold (rMT)	The resting motor threshold (rMT) will be measured by transcranial magnetic stimulation (TMS). rMT will be determined by measuring the motor evoked potential (MEP) in the abductor digiti	test days 2 and 4 (last day of treatment periods; approx. 5 hours after last intake of fampridine SR) to assess differences between the verum and placebo condition