University Hospital of Psychiatry Zurich
Zurich, Canton of Zurich, 8008, Switzerland
Location contact
Laura V. Schurek, M. Sc.
CONTACT
Prof. Dr. rer. nat. Boris B. Quednow, Dr. rer. nat.
CONTACT
NCT Number: NCT07532460
The study aims to address the neurobiological basis of cognitive impairments in chronic cocaine users by investigating the potential impact of an acute potassium channel blockade on working memory performance and other cognitive functions.
Trial opening soon.
Get Notified20 year–50 year
All sexes
Interventional
Not applicable
Zurich, Canton of Zurich, 8008, Switzerland
Laura V. Schurek, M. Sc.
CONTACT
Prof. Dr. rer. nat. Boris B. Quednow, Dr. rer. nat.
CONTACT
Chronic cocaine use is associated with impairments in cognitive functions, particularly in working memory, which are thought to contribute to the persistence of addictive behaviors and high relapse rates. Despite the clinical relevance of these cognitive deficits, the underlying neuropharmacological mechanisms remain insufficiently understood.
Preclinical and clinical evidence suggests that potassium channels may play an important role in the regulation of neuronal excitability and cognitive processes, including working memory. However, their contribution to cognitive impairments in individuals with cocaine use disorder has not yet been systematically investigated in humans.
The present study aims to investigate the role of potassium channel modulation in working memory performance in individuals with chronic cocaine use. The study addresses the following key research questions: (1) Does modulation of potassium channels influence working memory performance in individuals with chronic cocaine use? and (2) How are potential effects related to behavioral responses observed during the experimental sessions?
To address these questions, a randomized, controlled, cross-over study will be conducted in participants with a history of chronic cocaine use. Participants will complete a series of neurocognitive tasks assessing working memory and related cognitive domains under controlled experimental conditions. Blood samples will be collected at multiple time points to quantify substance levels and to support the interpretation of behavioral findings. The results of this study may contribute to a better understanding of the neurobiological mechanisms underlying cognitive impairments in cocaine use and inform future research on cognitive dysfunction in substance use disorders.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Two doses of fampridine administered during one of the two experimental test sessions.
Matching placebo administered during one of the two experimental test sessions.
Time frame: Baseline and during both experimental sessions
Working memory performance will be assessed using a cognitive test battery covering different domains of working memory, including visuo-spatial (Spatial Working Memory [SWM], total errors; Paired Associates Learning [PAL], first trial memory score) and verbal-numeric components (Letter Number Sequencing Task [LNST], total score; Letter N-Back Task, discrimination index d'). Individual test scores will be standardized (z-transformation) and combined into a global working memory score according to Vonmoos et al (2013).
Time frame: Baseline and during both experimental sessions
Neurofilament light chain (NfL), a marker of axonal integrity, and glial fibrillary acidic protein (GFAP), a marker of microglia activation, levels will be analysed to assess potential drug challenge-related brain structural remodelling or to predict the effect of potassium challenge blockade.
Time frame: Baseline and during both experimental sessions
Subjective ratings of current mood (affective state, stress) and craving, pre- and post-cue exposure.
Current affective state will be assessed using the Positive and Negative Affect Schedule (PANAS; positive affect range: 10-50, negative affect range: 10-50) and visual analog scales (VAS; range 0-100, with higher scores indicating greater levels) of affective state and stress burden.
Current cocaine craving will be assessed using the Cocaine Craving Questionnaire-Brief (CCQ-Brief; total score range: 10-70, with higher scores representing worse outcomes) and visual analog scales (VAS; range 0-100, with higher scores indicating greater levels) of craving intensity, distinguishing between wanting, needing and having the urge for cocaine.
Time frame: During both experimental sessions
Potential adverse effects of the study drug will be assessed using the List of Complaints and visual analog scales (VAS; range 0-100, with higher scores indicating greater levels) of perceived effects of the substance, dizziness, drowsiness, nausea and impaired concentration.
Time frame: During both experimental sessions
Plasma concentration of the study drug
Time frame: During both experimental sessions
Heart rate variability is recorded during the test sessions to measure the level of stress and to investigate whether the physiological strain of the test is reduced when taking the study drug.
Contact information is provided by the study sponsor or research team.
Laura V Schurek, M. Sc.
CONTACT
Prof. Dr. rer. nat. Boris B. Quednow, Dr. rer. nat.
CONTACT
Boris Quednow
Other
Randomised, Double-Blind, Placebo-Controlled, Crossover Study Investigating the Role of Potassium Channels in Working Memory Impairments of Chronic Cocaine Users
Acronym: POTCHICUD
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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