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Trial · NCT07532460

The Role of Potassium Channels in Working Memory Impairments of Chronic Cocaine Users

NCT07532460, Not applicable, Recruiting, Boris Quednow

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. The Role of Potassium Channels in Working Memory Impairments of Chronic Cocaine Users. Trials, record NCT07532460. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07532460

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Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title
The Role of Potassium Channels in Working Memory Impairments of Chronic Cocaine Users
NCT number
NCT07532460
Status
Recruiting
Phases
Not applicable
Enrollment
40 participants, estimated
Lead sponsor
Boris Quednow
Conditions
Cocaine Use Disorder (CUD), Cognitive Impairments
Interventions
4-aminopyridine (4-AP), Placebo
First posted
2026-04-16
Last updated
2026-08-17

Source ClinicalTrials.gov

Registered outcomes6

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryGlobal Working Memory PerformanceBaseline 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).
SecondaryNeurofilament light chain (NfL) and glial fibrillary acidic protein (GFAP)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.
SecondarySubjective ratings of current mood and cravingBaseline 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.
SecondaryAdverse effects of the study drugDuring 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.
SecondaryPlasma concentrationDuring both experimental sessionsPlasma concentration of the study drug
SecondaryHeart rate variabilityDuring both experimental sessionsHeart 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.

Outcomes0

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

None in this release.

Results by group0

Each measurement the trial posted, group by group, in the words and numbers it posted.

None in this release.

Participant flow0

How many started, completed or left each group, period by period.

None in this release.

Adverse events0

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

None in this release.

Adverse event totals0

The totals the trial posted for each group.

None in this release.

Papers0

The papers the trial lists on ClinicalTrials.gov.

None in this release.

Grants0

The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.

None in this release.

Trial comparisons0

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

None in this release.

Tests4

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

TestNamed asSource
1-Back TaskPrimary outcomeConductCognition
2-Back TaskPrimary outcomeConductCognition
Letter-Number Sequencing TaskPrimary outcomeConductCognition
Paired Associate LearningPrimary outcomeConductCognition

Data dates

The day each source was copied for this release.

ClinicalTrials.gov
2026-11-12
ClinicalTrials.gov
Results, from AACT
2026-03-23
AACT
NIH grant links
2026-11-13
NIH RePORTER

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

For software

Read this trial from software.

The record and each of its lists are JSON, twenty rows a page. No key.

GET https://conductscience.org/api/trials/v1/NCT07532460

GET https://conductscience.org/api/trials/v1/NCT07532460/registered