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Completed

NCT Number: NCT01164059

Clinical Effectiveness of Newer Antipsychotics in Comparison With Conventional Antipsychotics in Schizophrenia

This study is designed to compare the efficacy and drug tolerability of two strategies for the treatment of schizophrenia. The two strategies consist of utilizing, on the one hand, a conventional antipsychotic like haloperidol or flupentixol and, on the other hand, a newer antipsychotic compound like olanzapine, quetiapine or aripiprazole in patients with schizophrenia.

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Key information

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

Universitätsklinikum Aachen, Aachen, Germany

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About this study

There is agreement in the psychiatry community that the so-called atypical antipsychotics should be considered first choice in the treatment of schizophrenic disorders. However, the general superiority of these newer antipsychotic drugs over the older conventional drugs could not be clearly demonstrated in recent controlled clinical trials. The discrepancy between every day's clinical perception and the results of clinical trials raises the question whether the studies performed so far employed the adequate methodological approach to represent the daily practice situation which is characterized by a wide variety of duration and type of the schizophrenic disorder, concomitant diseases, and medications. Moreover, some studies might not have been focused adequately on patient-relevant outcome variables.

The present study project is designed to answer these open questions. The innovative character of the study design is

  • that different neuroleptic strategies will be compared rather than single antipsychotic drugs, using
  • an enhanced biometric design, that provides a choice of treatment with respect to the individual patient though the trial as such is randomised controlled and double blind;
  • that clinically relevant endpoints such as quality of life will be the primary variables, and
  • inclusion and exclusion criteria lead to a study population representing clinical every day practice as near as possible.

Another innovatory procedure is that serum levels of the study drugs will be recorded twice during the study. The authors hope that their design might yield transfer effects for other clinical trials facing similar problems.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Schizophrenia
  • age 18-65 years
  • necessity to establish new or change antipsychotic treatment due to unsatisfying results or side effects
  • written informed consent

Exclusion criteria

(amongst others):

  • Known or suspected hypersensitivity to olanzapine, quetiapine, aripiprazole, flupentixol or haloperidol
  • Acute suicidal tendency
  • "Einwilligungsvorbehalt (BGB)" or "Unterbringung (PsychKG)"
  • Epilepsy
  • Organic psychosis
  • Parkinson Disease
  • Dementia
  • History of malignant neuroleptic syndrome
  • QTc interval ≥ 0.5s / history of congenital QTc prolongation

Treatment and study plan

Olanzapine

Drug

Olanzapine 10, 15, or 20 mg / day

Flupentixol

Drug

Flupentixol 6, 9, or 12 mg / day

Quetiapine

Drug

Quetiapine 400, 600, or 800 mg / day

Aripiprazole

Drug

Aripiprazole 10, 15, or 20 mg / day

Haloperidol

Drug

Haloperidol 3, 4.5, or 6 mg / day

Primary outcomes

  1. Contentment with treatment: Patient (SF-36)

    Time frame: 24 weeks

  2. Contentment with treatment: Psychiatrist (CGI)

    Time frame: 24 weeks

Secondary outcomes

  1. Subscores of SF-36

    Time frame: 24 weeks

  2. Subjective wellbeing under neuroleptic treatment scale (SWN-K)

    Time frame: 24 weeks

  3. Positive and Negative Syndrome Scale (PANSS)

    Time frame: 24 weeks

Sponsors and collaborators

Lead sponsor

University of Bremen

Other

Collaborators

  • German Federal Ministry of Education and Research

Registry information

Official study title

Clinical Effectiveness Of The Newer Antipsychotic Compounds Olanzapine, Quetiapine And Aripiprazole In Comparison With Low Dose Conventional Antipsychotics (Haloperidol And Flupentixol) In Patients With Schizophrenia

Acronym: NeSSy

Important dates

Study start
2010
Primary completion
2013
Study completion
2014
First posted
Jul 16, 2010
Registry last updated
Jun 22, 2015

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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