Skip to content

Optimization of Acute Treatment in First Episode Schizophrenia

Optimization of Acute Treatment in First Episode Schizophrenic Patients by New Pharmacological Treatments

Status
UNKNOWN
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00157378
Enrollment
300
Registered
2005-09-12
Start date
2000-11-30
Completion date
2004-12-31
Last updated
2005-09-12

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

Conditions

Schizophrenia, First-Episode

Keywords

first episode,, schizophrenia,, atypical neuroleptics,, negative symptoms

Brief summary

The study is a multicenter, double-blind, randomized, parallel-group study with first episode schizophrenic patients. During a treatment phase of 8 weeks the patients are treated with Risperidone or Haloperidol. Aim of the project is to compare the effects of the atypical neuroleptic Risperidone with those of the conventional neuroleptic Haloperidol and to evaluate whether the assumed advantages of atypical neuroleptics compared to conventional neuroleptics are also present when both medications are administered in rather low daily dosages (min. 2 mg/d; max. 8 mg/d).

Detailed description

Considering that first episode schizophrenic patients compared to multiple episode patients respond to lower dosages of neuroleptics, the study aims to reach neuroleptic response under the lowest possible dosage of the study medication (haloperidol or risperidone). Therefore the initial dosage of the study medication is 2 mg/d. Depending on the patients' symptomatology, the daily dosage of the study medication can be increased by 2 mg in weekly intervals up to a maximum dosage of 8 mg/d. Patients with the diagnosis of schizophrenia (F20, according to ICD-10-criteria) are consecutively enrolled in the study. The patients are assessed at weekly intervals during the acute inpatient treatment phase of 8 weeks. Apart from the weekly psychopathological characterisation additionally neuropsychobiological data are assessed at the time of admission and at the end of the study. Major questions of the study are, whether patients, who have been treated with risperidone compared with those, who have been treated with haloperidol show a better treatment outcome regarding negative symptoms and exhibit fewer extra-pyramidal motor side effects. Furthermore it is hypothesised, that the treatment with Risperidone has better effects on cognitive disorders/dysfunctions and depressive symptoms and that the patients, who receive Risperidone are more compliant and have a higher quality of life.

Interventions

DRUGRisperidone, Haloperidol

Sponsors

Janssen-Cilag Ltd.
CollaboratorINDUSTRY
German Research Network On Schizophrenia
CollaboratorNETWORK
Department of Psychiatry University of Bonn
CollaboratorOTHER
Heinrich-Heine University, Duesseldorf
CollaboratorOTHER
Department of Psychiatry University FU Berlin
CollaboratorOTHER
University of Göttingen
CollaboratorOTHER
University of Cologne
CollaboratorOTHER
Mainz University
CollaboratorOTHER
University Hospital Tuebingen
CollaboratorOTHER
Universität Duisburg-Essen
CollaboratorOTHER
University of Mannheim
CollaboratorOTHER
University of Jena
CollaboratorOTHER
Martin-Luther-Universität Halle-Wittenberg
CollaboratorOTHER
RWTH Aachen University
CollaboratorOTHER
University of Wuerzburg
CollaboratorOTHER
Ludwig-Maximilians - University of Munich
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE

Eligibility

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

Inclusion criteria

* ICD-10 criteria for first episode schizophrenia * age between 18 and 55 * informed consent

Exclusion criteria

* legal reasons * insufficient knowledge of the german language * substance abuse or addiction * pregnancy * serious physical illness * organic brain disease * contraindication to neuroleptic treatment

Design outcomes

Primary

MeasureTime frame
weekly assessment of psychopathology (e.g.PANSS)and side-effects

Secondary

MeasureTime frame
cognitive disability
depression
life quality at time of admission & end of study

Countries

Germany

Outcome results

None listed

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