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Clinical Registry of Patients Under Treatment With Atypical Antipsychotics

Clinical Registry of Patients Under Treatment With Atypical Antipsychotics

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02409823
Enrollment
665
Registered
2015-04-07
Start date
2015-02-28
Completion date
2015-08-31
Last updated
2015-10-20

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

Conditions

Bipolar Depressive Disorder, Major Depressive Disorder, Parkinson's Disease With Hallucinations, Schizophrenia

Keywords

adverse drug reactions, adherence to treatment, quality of life, clinical status

Brief summary

Antipsychotic drugs are characterized by blocking dopaminergic D2 receptors. They have been found to be effective and safe for the treatment of schizophrenia, bipolar disorders, depressive episodes associated with bipolar disorder, or psychotic symptoms in the context of Parkinson's disease. Atypical antipsychotics have lower blocking potency on D2 receptors, at the time that interact with serotoninergic, adrenergic and histaminergic receptors, among others. Quetiapine extended-release has the same clinical efficacy as the immediate-release formulation, but reduces the amount of daily doses, possibly contributing to increased treatment adherence. The purpose of this registry is to explore adherence to treatment, the occurrence of adverse drug reactions and the clinical outcomes in a sample of patients under treatment with atypical antipsychotics in several Central American countries. For this study, clinical data will be extracted from the medical records of 1000 patients with schizophrenia, depressive disorders or Parkinson's Disease with hallucinations. Occurrence of adverse drug reactions, namely weight gain, somnolence, extrapyramidal reactions and symptoms of orthostatic hypotension; adherence to treatment; and changes in quality of life and clinical status will be assessed during the first 8 weeks of treatment.

Interventions

any atypical antipsychotic

Sponsors

Pontifical Catholic University of Argentina
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

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

Inclusion criteria

* at least 18 years-old * have a diagnosis of schizophrenia, major depressive disorder, bipolar depressive disorder, parkinson's disease with hallucination * such patients should receive antipsychotics as their usual treatment * they should give informed consent before participating

Exclusion criteria

* no treatment with atypical antypsichotics * other diseases

Design outcomes

Primary

MeasureTime frame
Occurrence of Adverse Drug Reactions8 weeks
Adherence to treatment8 weeks

Secondary

MeasureTime frame
Quality of Life8 weeks
Clinical status (CGI score)8 weeks

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 13, 2026