← Eichor
Study identifier: NCT06751784 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Cross-over Study on the Influence of Fampridine on Working Memory in Mild to Moderate Depression

Condition: Working Memory · Mild to Moderate Depression  ·  Sponsor: University of Basel

PhasePhase 2
Planned participants38
Who can joinAll sexes, 18 Years to 55 Years
Healthy volunteersNo

About this study

Cognitive deficits, including working memory deficits, are often present in depression and there are currently no effective pharmacological treatments targeting working memory deficits. Papassotiropoulos et al. (2024) has recently demonstrated that fampridine, a potassium channel blocker, can enhance working memory in healthy individuals with lower baseline performance, suggesting it may hold potential for addressing cognitive deficits in clinical populations. The primary aim of this study is to evaluate whether fampridine improves working memory performance in mild to moderate depression

This description comes directly from the study's public registry record.

Talk to the study team

Christiane Gerhards, MD  ·  +41 61 207 0244  ·  christiane.gerhards@unibas.ch

Always discuss trial participation with your own doctor first.

Locations (1)

University of Basel, Reserach Cluster Molecular and Cognitive NeurosciencesBasel, Canton of Basel-City, SwitzerlandRecruiting

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT06751784