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NCT Number: NCT00918021

Polypharmacy in Clozapine-resistant Schizophrenia

The aim of this randomized, double-blind study is to verify the hypothesis that clozapine monotherapy is as efficient as a combination of clozapine and olanzapine therapy in treatment-resistant schizophrenia.

A third of schizophrenia patients are non -responders to medications used nowadays. These patients are usually treated with clozapine, but a large proportion of patients don't recover sufficiently. Therefore, these patients are treated with combination of two or more drugs to achieve better treatment results. Until now the scientific evidence has been insufficient to assess the utility of polypharmacy.

The aim is to study during 2009 with voluntary patients, if there is any benefit of olanzapine augmentation compared with pure clozapine monotherapy. During the study the patients are not exposed to any additional intervention. The intervention in this study is just to reduce the previously used polypharmacy.

Methods: This study lasts for 24 weeks. Participants (30) are randomized in one of two alternative interventions (A or B) before the study. After 12 weeks the intervention arms cross over (from A to B and from B to A).

Group B: In addition to clozapine, the participants receive their normal dosage of olanzapine (=the same as on the hospital ward) for 12 weeks, next the decreasing dosage of olanzapine for four weeks and subsequently placebo for 8 weeks

Group A: : In addition to clozapine the participants receive the decreasing dosage of olanzapine for four weeks, next placebo for 8 weeks, after that the increasing dosage of olanzapine for four weeks and subsequently the normal dosage of olanzapine for 8 weeks

The response for the medical treatment is assessed by Clinical Global Improvement Scale (CGIS) and Global Assessment of Functioning (GAF) -scale.

The primary outcomes are GAF and modified CGIS during the parallel phase of the study (the first 12 weeks). The second phase (the last 12 weeks) of the cross-over study is used in the secondary analysis. The use of additional medication (such as benzodiazepines) is used as a secondary outcome measure.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

Niuvanniemi Hospital

Kuopio, FI-70240, Finland

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • age ≥18 years, (adult), legally competent
  • the patient is able to understand the purpose of the study and is eligible to sign the written informed consent form.
  • insufficient response to the valid clozapine-olanzapine -polypharmacy
  • psychotropic medication has been constant (unchangeable) during the past 2 months

Exclusion criteria

  • Pregnancy

Treatment and study plan

Olanzapine

Drug

normal dosage of olanzapine (the same dosage as on hospital ward)

Other names: Solazin

Placebo

Drug

placebo

Primary outcomes

  1. The primary outcomes are GAF and modified CGIS during the parallel phase of the study (the first 12 weeks).

    Time frame: 0, 12, 24 weeks

Secondary outcomes

  1. The second phase (the last 12 weeks) of the cross-over study is used in the secondary analysis. The use of additional medication (such as benzodiazepines) is used as a secondary outcome measure.

    Time frame: 0, 12, 24 weeks

Sponsors and collaborators

Lead sponsor

Niuvanniemi Hospital

Other

Registry information

Official study title

Olanzapine Augmentation in Clozapine-resistant Schizophrenia: a Randomized Double-blind Study

Acronym: CLOZANS

Important dates

Study start
2009
Primary completion
2010
Study completion
2010
First posted
Jun 11, 2009
Registry last updated
Nov 19, 2010

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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