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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00159133
Other study ID # 01GI 9932 - P 2.2.2.2
Secondary ID
Status Completed
Phase Phase 4
First received September 7, 2005
Last updated January 28, 2008
Start date November 2001
Est. completion date June 2006

Study information

Verified date January 2008
Source Heinrich-Heine University, Duesseldorf
Contact n/a
Is FDA regulated No
Health authority Germany: Federal Institute for Drugs and Medical Devices
Study type Interventional

Clinical Trial Summary

Prodrome based early intervention with an antipsychotic drug vs. benzodiazepine was applied in patients with first episode schizophrenia after one year neuroleptic maintenance treatment. Two groups of patients were followed over a period of 1 year: one further on under maintenance neuroleptic treatment, the other one after stepwise drug discontinuation.


Description:

In case of early signs of a relapse prodrome based early intervention with an antipsychotic drug (Haloperidol, Risperidone and other) vs. benzodiazepine (Lorazepam) was applied in patients with first episode schizophrenia after one year neuroleptic maintenance treatment. Two groups of patients were followed over a period of 1 year: one further on under maintenance neuroleptic treatment (Haloperidol, Risperidone and other) , the other one after stepwise drug discontinuation.


Recruitment information / eligibility

Status Completed
Enrollment 71
Est. completion date June 2006
Est. primary completion date June 2006
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 55 Years
Eligibility Inclusion Criteria:

- First-episode in schizophrenia (according ICD-10 F20)

- Age between 18 and 55

- Informed consent

- One year neuroleptic maintenance treatment

Exclusion Criteria:

- Residence outside of the catchment area

- Legal reasons

- Insufficient knowledge of the german language

- Substance abuse or addiction

- Pregnancy

- Serious physical illness

- Organic brain disease

- Contraindication to neuroleptic treatment

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Drug:
antipsychotics vs. Lorazepam (Drugs)
Early intervention with low-dose antipsychotics vs. lorazepam (up to 3 mg/day) in case of early warning signs of an impending relapse;

Locations

Country Name City State
Germany German Research Network on Schizophrenia, Department of Psychiatry and Psychotherapy at the Heinrich-Heine-University Düsseldorf Düsseldorf North Rhine-Westphalia

Sponsors (17)

Lead Sponsor Collaborator
Heinrich-Heine University, Duesseldorf German Federal Ministry of Education and Research, German Research Network On Schizophrenia, Humboldt-Universität zu Berlin, Janssen-Cilag Ltd., Ludwig-Maximilians - University of Munich, Mainz University, Martin-Luther-Universität Halle-Wittenberg, RWTH Aachen University, Universität Duisburg-Essen, University Hospital Tuebingen, University of Bonn, University of Cologne, University of Göttingen, University of Jena, University of Mannheim, University of Wuerzburg

Country where clinical trial is conducted

Germany, 

References & Publications (1)

Gaebel W, Möller HJ, Buchkremer G, Ohmann C, Riesbeck M, Wölwer W, Von Wilmsdorff M, Bottlender R, Klingberg S. Pharmacological long-term treatment strategies in first episode schizophrenia--study design and preliminary results of an ongoing RCT within the German Research Network on Schizophrenia. Eur Arch Psychiatry Clin Neurosci. 2004 Apr;254(2):129-40. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary relapse rate 1 year No
Secondary psychopathology 1 year No
Secondary social and cognitive functioning 1 year No
Secondary side-effects 1 year Yes
Secondary drop-out 1 year No
Secondary quality of life 1 year No
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