Comparison of Antipsychotic Combination Treatment of Olanzapine and Amisulpride to Monotherapy (COMBINE)
Primary Purpose
Schizophrenia, Schizoaffective Disorder
Status
Completed
Phase
Phase 4
Locations
Germany
Study Type
Interventional
Intervention
Olanzapine
Amisulpride
Olanzapine and Amisulpride
Sponsored by
About this trial
This is an interventional treatment trial for Schizophrenia focused on measuring schizophrenia, amisulpride, olanzapine, polypharmacy
Eligibility Criteria
Inclusion Criteria:
- Patients with schizophrenia and schizoaffective disorder according to International Classification of Diseases (ICD-10);
- age 18-65;
- Positive and Negative Symptom Scale Total-Score ≥ 70 and two items of the positive symptom subscale ≥4.
- voluntary treatment after written informed consent
- legal capacity
- exclusion of pregnancy by laboratory test (Beta HCG)
Exclusion Criteria:
- participation in other interventional studies with drugs or medical devices
- first episode patients
- physical disease that might have effects on the conduct or evaluation of the trial
- contraindications to medication according to experts information
- oversensitivity to active substance or other component of the drugs used
- known clozapine resistance
- suicidal ideation
- pregnancy or lactation
- which of pregnancy or absence save contraception
- dependency to sponsor or investigator
- institutionalization through judicial or regulatory order
- oversensitivity to placebo (mannite/aerosil)
Sites / Locations
- RWTH Aachen
- Rheinhessen Fachklinik Alzey
- Rhein-Mosel-Fachklinik Andernach
- Bezirkskliniken Schwaben, Bezirkskrankenhaus Augsburg
- Charite-Universitätsmedizin Berlin
- LWL-Klinik Dortmund
- LVR-Klinikum Düsseldorf
- Zentrum für Seelische Gesundheit Kreiskliniken Darmstadt-Dieburg Standort: Groß-Umstadt
- Universitätsmedizin Göttingen
- Klinik für Psychiatrie, Psychotherapie und Psychosomatik am Bezirkskrankehaus Günzburg
- Klinik für Psychiatrie, Sozialpsychiatrie und Psychotherapie Medizinische Hochschule Hannover (MHH)
- Universitätsklinikum Heidelberg
- LVR-Klinikum Köln
- LVR-Klinik Langenfeld
- Universitätsklinikum Leipzig, Klinik und Poliklinik für Psychiatrie und Psychotherapie
- Universitätsmedizin Mainz Klinik für Psychiatrie und Psychotherapie
- Zentralinstitut für Seelische Gesundheit
- LMU München
- TU München
- Bezirksklinikum Regensburg, Klinik für Psychiatrie und Psychotherapie
- Universitätsklinikum Würzburg
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Active Comparator
Active Comparator
Active Comparator
Arm Label
Olanzapine or Placebo
Amisulpride or Placebo
Olanzapine and Amisulpride
Arm Description
Outcomes
Primary Outcome Measures
Symptomatic improvement of schizophrenia after 8 weeks of treatment in comparison to time of inclusion of patient measured py Positive and Negative Symptom Scale (PANSS)
Whether there is a symptomatic improvement of schizophrenia after 8 weeks of treatment in comparison to time of inclusion of patient measured py Positive and Negative Symptom Scale (PANSS)
Secondary Outcome Measures
Symptomatic improvement of schizophrenia after 16 weeks of treatment in comparison to time of inclusion of patient measured py PANSS total score reduction
To study whether a combination treatment of olanzapine and amisulpride show a PANSS total score reduction from baseline to week 16.
Symptomatic improvement of schizophrenia from baseline to week 2 up to week 16 measured by PANSS total score reduction.
Whether a combination treatment of olanzapine and amisulpride show a PANSS total score reduction from baseline to every 2 weeks up to week 16.
PANSS total score reduction from baseline to week 2 as a predictor of the change after 8 weeks
Whether a change of PANSS total score reduction from baseline to week 2 is a predictor of the change after 8 weeks
Serious adverse drug reactions
Frequency and severity of serious adverse drug reactions
Change of clinical condition measured by Clinical Global Impression Scale (CGI scale)
Whether there is a change of clinical condition measured by Clinical Global Impression Scale (CGI scale)
Change of the subjective well-being measured by Subjective Wellbeing under Neuroleptics Scale (SWN-K)
Whether there is a change of the subjective well-being measured by Subjective Wellbeing under Neuroleptics Scale(SWN-K)
Full Information
NCT ID
NCT01609153
First Posted
May 23, 2012
Last Updated
April 15, 2019
Sponsor
Heinrich-Heine University, Duesseldorf
1. Study Identification
Unique Protocol Identification Number
NCT01609153
Brief Title
Comparison of Antipsychotic Combination Treatment of Olanzapine and Amisulpride to Monotherapy
Acronym
COMBINE
Official Title
A Randomized Double-blind Controlled Trial to Assess the Benefits of Olanzapine and Amisulpride Combination Treatment in Acutely Ill Schizophrenia Patients. - COMBINE
Study Type
Interventional
2. Study Status
Record Verification Date
April 2019
Overall Recruitment Status
Completed
Study Start Date
June 2012 (Actual)
Primary Completion Date
April 2019 (Actual)
Study Completion Date
April 2019 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Heinrich-Heine University, Duesseldorf
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
A study to examine whether an antipsychotic combination treatment of olanzapine and amisulpride is more effective than olanzapine and amisulpride alone.
Detailed Description
Polypharmacy in antipsychotic therapy is an important issue when treating patients with schizophrenia. It is not well confirmed that a combination of two antipsychotic drugs lead to therapeutic benefit in contrast to monotherapy. However there is a highly frequent practice of combining atypical non-clozapine treatment that could be due to potential benefits when seeking alternatives to a high rate of non-response in acute phase. Therefore there is a need for further trials of sufficient power to address efficacy and safety issues of this regimen. Combining two selected atypical drugs in a complementary way may minimize side-effects and enhance efficacy. In order to specify these advantages it is intend to examine approaches to combination treatment: Amisulpride and olanzapine show complementing receptor binding profiles and have shown to have efficacy and good tolerability when administered in combination in retrospective studies. The object of this trial is to study whether acutely ill patients with combination of amisulpride and olanzapine are more frequently in symptomatic remission after 8 weeks than those with olanzapine or amisulpride monotherapy.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Schizophrenia, Schizoaffective Disorder
Keywords
schizophrenia, amisulpride, olanzapine, polypharmacy
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
328 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Olanzapine or Placebo
Arm Type
Active Comparator
Arm Title
Amisulpride or Placebo
Arm Type
Active Comparator
Arm Title
Olanzapine and Amisulpride
Arm Type
Active Comparator
Intervention Type
Drug
Intervention Name(s)
Olanzapine
Other Intervention Name(s)
Zyprexa
Intervention Description
Coated tablet 5-20 mg milligram(s) per day for 16 weeks
Intervention Type
Drug
Intervention Name(s)
Amisulpride
Other Intervention Name(s)
Amisulprid Hexal
Intervention Description
200-800 mg milligram(s)per day for 16 weeks
Intervention Type
Drug
Intervention Name(s)
Olanzapine and Amisulpride
Other Intervention Name(s)
Zyprexa, Amisuprid Hexal
Intervention Description
Zyprexa:
Coated tablet 5-20 mg milligram(s) per day for 16 weeks
Amisulpride:
Coated tablet 200-800 mg milligram(s)per day for 16 weeks
Primary Outcome Measure Information:
Title
Symptomatic improvement of schizophrenia after 8 weeks of treatment in comparison to time of inclusion of patient measured py Positive and Negative Symptom Scale (PANSS)
Description
Whether there is a symptomatic improvement of schizophrenia after 8 weeks of treatment in comparison to time of inclusion of patient measured py Positive and Negative Symptom Scale (PANSS)
Time Frame
8 weeks
Secondary Outcome Measure Information:
Title
Symptomatic improvement of schizophrenia after 16 weeks of treatment in comparison to time of inclusion of patient measured py PANSS total score reduction
Description
To study whether a combination treatment of olanzapine and amisulpride show a PANSS total score reduction from baseline to week 16.
Time Frame
16 weeks.
Title
Symptomatic improvement of schizophrenia from baseline to week 2 up to week 16 measured by PANSS total score reduction.
Description
Whether a combination treatment of olanzapine and amisulpride show a PANSS total score reduction from baseline to every 2 weeks up to week 16.
Time Frame
Every 2 weeks up to week 16.
Title
PANSS total score reduction from baseline to week 2 as a predictor of the change after 8 weeks
Description
Whether a change of PANSS total score reduction from baseline to week 2 is a predictor of the change after 8 weeks
Time Frame
8 weeks
Title
Serious adverse drug reactions
Description
Frequency and severity of serious adverse drug reactions
Time Frame
16 weeks
Title
Change of clinical condition measured by Clinical Global Impression Scale (CGI scale)
Description
Whether there is a change of clinical condition measured by Clinical Global Impression Scale (CGI scale)
Time Frame
every 2 weeks from baseline up to week 16
Title
Change of the subjective well-being measured by Subjective Wellbeing under Neuroleptics Scale (SWN-K)
Description
Whether there is a change of the subjective well-being measured by Subjective Wellbeing under Neuroleptics Scale(SWN-K)
Time Frame
between week 0, 8, 16
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patients with schizophrenia and schizoaffective disorder according to International Classification of Diseases (ICD-10);
age 18-65;
Positive and Negative Symptom Scale Total-Score ≥ 70 and two items of the positive symptom subscale ≥4.
voluntary treatment after written informed consent
legal capacity
exclusion of pregnancy by laboratory test (Beta HCG)
Exclusion Criteria:
participation in other interventional studies with drugs or medical devices
first episode patients
physical disease that might have effects on the conduct or evaluation of the trial
contraindications to medication according to experts information
oversensitivity to active substance or other component of the drugs used
known clozapine resistance
suicidal ideation
pregnancy or lactation
which of pregnancy or absence save contraception
dependency to sponsor or investigator
institutionalization through judicial or regulatory order
oversensitivity to placebo (mannite/aerosil)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Christian Schmidt-Kraepelin, Dr.
Organizational Affiliation
Heinrich-Heine University, Duesseldorf
Official's Role
Principal Investigator
Facility Information:
Facility Name
RWTH Aachen
City
Aachen
ZIP/Postal Code
52074
Country
Germany
Facility Name
Rheinhessen Fachklinik Alzey
City
Alzey
ZIP/Postal Code
55232
Country
Germany
Facility Name
Rhein-Mosel-Fachklinik Andernach
City
Andernach
ZIP/Postal Code
56626
Country
Germany
Facility Name
Bezirkskliniken Schwaben, Bezirkskrankenhaus Augsburg
City
Augsburg
ZIP/Postal Code
89156
Country
Germany
Facility Name
Charite-Universitätsmedizin Berlin
City
Berlin
ZIP/Postal Code
10117
Country
Germany
Facility Name
LWL-Klinik Dortmund
City
Dortmund
ZIP/Postal Code
44281
Country
Germany
Facility Name
LVR-Klinikum Düsseldorf
City
Düsseldorf
ZIP/Postal Code
40629
Country
Germany
Facility Name
Zentrum für Seelische Gesundheit Kreiskliniken Darmstadt-Dieburg Standort: Groß-Umstadt
City
Groß-Umstadt
ZIP/Postal Code
64823
Country
Germany
Facility Name
Universitätsmedizin Göttingen
City
Göttingen
ZIP/Postal Code
37075
Country
Germany
Facility Name
Klinik für Psychiatrie, Psychotherapie und Psychosomatik am Bezirkskrankehaus Günzburg
City
Günzburg
ZIP/Postal Code
89312
Country
Germany
Facility Name
Klinik für Psychiatrie, Sozialpsychiatrie und Psychotherapie Medizinische Hochschule Hannover (MHH)
City
Hannover
ZIP/Postal Code
30625
Country
Germany
Facility Name
Universitätsklinikum Heidelberg
City
Heidelberg
ZIP/Postal Code
69115
Country
Germany
Facility Name
LVR-Klinikum Köln
City
Köln
ZIP/Postal Code
51109
Country
Germany
Facility Name
LVR-Klinik Langenfeld
City
Langenfeld
ZIP/Postal Code
40764
Country
Germany
Facility Name
Universitätsklinikum Leipzig, Klinik und Poliklinik für Psychiatrie und Psychotherapie
City
Leipzig
ZIP/Postal Code
04103
Country
Germany
Facility Name
Universitätsmedizin Mainz Klinik für Psychiatrie und Psychotherapie
City
Mainz
ZIP/Postal Code
55131
Country
Germany
Facility Name
Zentralinstitut für Seelische Gesundheit
City
Mannheim
ZIP/Postal Code
68159
Country
Germany
Facility Name
LMU München
City
München
ZIP/Postal Code
80336
Country
Germany
Facility Name
TU München
City
München
ZIP/Postal Code
81675
Country
Germany
Facility Name
Bezirksklinikum Regensburg, Klinik für Psychiatrie und Psychotherapie
City
Regensburg
ZIP/Postal Code
93053
Country
Germany
Facility Name
Universitätsklinikum Würzburg
City
Würzburg
ZIP/Postal Code
97080
Country
Germany
12. IPD Sharing Statement
Citations:
PubMed Identifier
35276079
Citation
Schmidt-Kraepelin C, Feyerabend S, Engelke C, Riesbeck M, Meisenzahl-Lechner E, Verde PE, Correll CU, Kluge M, Makiol C, Neff A, Lange C, Englisch S, Zink M, Langguth B, Poeppl TB, Reske D, Gouzoulis-Mayfrank E, Grunder G, Hasan A, Brockhaus-Dumke A, Jager M, Baumgartner J, Leucht S, Cordes J; COMBINE Study Group. Amisulpride and olanzapine combination treatment versus each monotherapy in acutely ill patients with schizophrenia in Germany (COMBINE): a double-blind randomised controlled trial. Lancet Psychiatry. 2022 Apr;9(4):291-306. doi: 10.1016/S2215-0366(22)00032-3. Epub 2022 Mar 8.
Results Reference
derived
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Comparison of Antipsychotic Combination Treatment of Olanzapine and Amisulpride to Monotherapy
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