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Cognitive Effects of Nimodipine in Patients With Schizophrenia

Cognitive Effects of Nimodipine in Patients With Schizophrenia

Status
Completed
Phases
Early Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03671525
Enrollment
18
Registered
2018-09-14
Start date
2018-10-05
Completion date
2023-05-12
Last updated
2023-06-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Schizo Affective Disorder, Schizophrenia

Brief summary

This study aims to evaluate the acute effects of nimodipine on cognitive performance in patients with schizophrenia using a battery of cognitive assessments.The subjects will also complete a 30-minute structural and functional MRI scan, with the goal of linking brain activity with working memory performance. Investigators predict that the performance increase induced by nimodipine will be greater in subjects who carry the A allele for the Calcium Voltage-Gated Channel Subunit Alpha1 C (CACNA1C) risk single nucleotide polymorphism (SNP) (rs1006737) in comparison to the response of G carriers.

Detailed description

The main cognitive task of interest in this study is the N-back task because of the observed attenuation of prefrontal and parietal cortical activity after nimodipine administration in healthy subjects. Investigators hypothesize that acute nimodipine administration will improve cortical activation, which will lead to improved cognitive performance. The current study will provide insight whether nimodipine or another calcium channel blocker could be used as a treatment approach to alleviate cognitive deficits in patients with schizophrenia.

Interventions

DRUGNimodipine

Subject will receive two 30mg capsules of nimodipine during study visit.

DRUGPlacebo oral capsule

Two coconut oil capsules that mimic the size and color of the nimodipine capsules

Sponsors

Johns Hopkins University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
OTHER
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 55 Years
Healthy volunteers
No

Inclusion criteria

* This study will recruit patients with schizophrenia and/or schizoaffective disorder

Exclusion criteria

* past or current neurological disorder (including stroke, brain tumor, epilepsy, Alzheimer's, Parkinson's or Huntington's disease) * uncontrolled medical disorder * current or past hypotension * head trauma with loss of consciousness in the last year or any evidence of functional impairment due to and persisting after head trauma * positive pregnancy test, or currently breast feeding * having an adverse reaction to nimodipine, or other calcium channel blocker

Design outcomes

Primary

MeasureTime frameDescription
Brain activity as assessed by BOLD fMRIbetween 30 min and 1 hour after doseparticipants will complete an MRI scan to link brain activity with cognitive performance. Measures will be recorded in Arbitrary units.
Changes in Visual Learning and Memory Scoreapproximately an hour after doseParticipants will complete the Brief Visuospatial Memory Task - Revised (BVMT-R) before and after administration of drug or placebo to determine the effect of nimodipine on visuospatial memory in patients with schizophrenia. Scores range from 0 to 60, with higher values indicating better performance. Administration takes approximately 45 minutes to complete (including a 25 minute delay)
Changes in Auditory Learning and Memory Scoreapproximately an hour after doseDuring each study visit, participants will complete the Hopkins Verbal Learning Task - Revised (HVLT-R) before and after administration of drug or placebo to determine the effect of nimodipine on verbal learning and memory in patients with schizophrenia. Scores range from 0 to 60, with higher values indicating better performance. Administration takes approximately 35 minutes to complete (including a 20-25 minute delay).
Changes in Global Neurocognitive effect as assessed by the Global Neurocognitive Assessment (GNA)approximately an hour after doseDuring each study visit, participants will complete the Global Neurocognitive Assessment (GNA) before and after administration of drug or placebo to determine the effect of nimodipine on a range of neurocognitive measures in patients with schizophrenia. The GNA contains 10 items with varying score ranges. Higher scores indicate better performance.

Secondary

MeasureTime frameDescription
Effect of CACNA1C genotype on cognitive performance measuresduring 2-3 hour study visitThe CACNA1C risk-associated SNP (rs1006737) will be tested using a linear regression (with copy of A alleles) with each cognitive domain score to determine if CACNA1C genetics impact response to nimodipine.
Broader genetic associations with cognitive performanceduring 2-3 hour study visitGenetic data will be used more broadly to include testing of the effects of genetic variation including but not limited to schizophrenia, cognition, behavior, and drug metabolism.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026