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The Effect of Nitric Oxide on Spatial Working Memory in Patients With Schizophrenia - Pilot Study

The Effect of Nitric Oxide on Spatial Working Memory in Patients With Schizophrenia - Pilot Study

Status
Completed
Phases
Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02176044
Enrollment
21
Registered
2014-06-26
Start date
2014-08-31
Completion date
2016-02-29
Last updated
2016-03-09

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

Conditions

Schizophrenia

Keywords

Nitric Oxide, Sodium Nitroprusside, Spatial Working Memory, Psychosis, Schizophrenia

Brief summary

Spatial working memory (ability to remember where objects are in space) is impaired in patients with schizophrenia. It is thought that this impairment occurs due to problems with the chemical messenger (neurotransmitter), glutamate, and the N-methyl-D-aspartate (NMDA) glutamate receptor, particularly in the hippocampal brain region. NMDA receptor activation leads to increases in the release of the second messenger Nitric Oxide. Impaired NMDA receptor function would therefore be predicted to lead to reductions in Nitric Oxide production. Recent work suggests that a drug, sodium nitroprusside, which releases nitric oxide, enhances some aspects of cognition in schizophrenia (specifically related to negative symptoms). In this study, the investigators will test the hypothesis that sodium nitroprusside improves spatial working memory in patients with schizophrenia. 15 patients will receive sodium nitroprusside, and 15 will receive a nonactive compound (placebo). Their performance on a spatial working memory task will be tested before and after administration of sodium nitroprusside or placebo.

Interventions

Sponsors

King's College London
Lead SponsorOTHER

Study design

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

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

Patients with a diagnosis of schizophrenia or schizoaffective disorder, currently experiencing an exacerbation of symptoms (a score \> 20 for PANSS-Positive subscale), currently taking antipsychotics and who have given informed consent to participate.

Exclusion criteria

History of hypertension or current resting systolic blood pressure greater than 140 mmHg or diastolic blood pressure greater than 90 mmHg. Relevant medical illness (renal, hepatic, cardiac), prior history of intolerance to sodium nitroprusside, presence of a seizure disorder, any change in psychotropic medication in previous 6 weeks, diagnosis of substance abuse, pregnancy (as determined by urine test) or breastfeeding.

Design outcomes

Primary

MeasureTime frameDescription
Spatial Working Memory4 hours post-infusionperformance on Cambridge Neuropsychological Test Automated Battery spatial working memory task

Secondary

MeasureTime frameDescription
Brief Psychiatric Rating Scale (BPRS)4 hours post-infusionSymptoms rated on BPRS
Quick Inventory of Depressive Symptomatology (QIDS)4 hours post-infusionSymptoms rated on QIDS
Hypomania Checklist (HCL-32)4 hours post-infusionRating of symptoms on HCL-32
Positive and Negative Syndrome Scale (PANSS)4 hours post-infusionSymptoms rated on PANSS
Heart rate4 hours post-infusionHeart rate change from baseline
Respiratory rate4 hours post-infusionchange in respiratory rate from baseline.
Blood pressure4 hours post-infusionMeasurement of blood pressure.

Countries

United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 12, 2026