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Schizotypal Personality Disorder Risperidone

Status
Completed
Phases
Phase 1Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02535156
Enrollment
21
Registered
2015-08-28
Start date
2003-01-31
Completion date
2015-01-31
Last updated
2017-08-11

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

Conditions

Schizotypal Personality Disorder

Brief summary

Neurophysiological indices of self-monitoring were assessed in a group of patients with Schizotypal Personality Disorder (SPD) and a control group. Both groups were assessed after the administration of risperidone and placebo.

Detailed description

The electroencephalogram (EEG) was recorder while participants (SPD participants and controls) performed a behavioral task: the Eriksen Flanker Task. The continuous EEG was segmented, corrected for artifacts and averaged. A component of the event-related brain potential known as the error-related negativity (ERN) was identified and its amplitude quantified in microvolts. This procedure was conducted two hours after the administration of risperidone 1 mg and placebo (lactose) on two different experimental days and for each participant group (SPD patients and controls). The amplitude of the ERN after placebo was compared between groups to test for baseline (non-drug-induced) differences between patients and controls. The impact of risperidone on the amplitude of the ERN was compared between the two participant groups.

Interventions

DRUGRisperidone

1 mg Risperidone

DRUGPlacebo

Lactose Placebo

Sponsors

Fundació Institut de Recerca de l'Hospital de la Santa Creu i Sant Pau
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
BASIC_SCIENCE
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Schizotypal Personality Disorder

Exclusion criteria

* Major Psychiatric Disorder * Medical condition

Design outcomes

Primary

MeasureTime frameDescription
Neurophysiological indices of self-monitoring (Error Related Negativity)During acute effects of pharmacological treatment (up to 2 hours)Amplitude of the Error Related Negativity was assessed prior to and 2 hours after treatment administration

Outcome results

None listed

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