Comparative Efficacy and Acceptability of Antimanic Drugs in Acute Mania

Sponsor
Guiyun Xu (Other)
Overall Status
Unknown status
CT.gov ID
NCT01893229
Collaborator
The University of Hong Kong (Other)
120
2
6
27
60
2.2

Study Details

Study Description

Brief Summary

Background:

Bipolar disorder is one of the most common mental illnesses affecting 1%-4% of the population, and one of the leading causes of worldwide disability. Mania is a condition of excessively elevated mood, characterizes bipolar disorder, and usually is a main cause of hospitalization. Mood stabilisers and antipsychotic drugs have long been the maintenance treatment of acute mania with and without psychotic symptoms. Though clinical trails have been demonstrated that these drugs are individually more effective than placebo in the relatively long term (e.g 4, 8 weeks). However, in the pragmatic practice, patient at acute mania urgently want to see the effectiveness, and psychiatrist under great pressure and are in great need to evaluate the very short-term effectiveness (e.g one week). If the first attempted antimanic drug fails, psychiatrist need the evidence that which medication should be to added on or switch to.

Objectives:

one main aim is to rank the short-term ( e.g.one and two week) effectiveness and acceptability of the common anti-mania drugs, including Lithium, Valproate, Oxcarbazepine, Quetiapine, Olanzapine, or Ziprasidone. Secondary aim is to investigate which medication to add on for non-responders or switch to.

Methods:

The study setting: it is expected that 120 subjects with a diagnose of DSM-IV bipolar I disorder will be recruited from Guangzhou Psychiatric Hospital, the earliest psychiatric hospital in the history of China established by Dr.J. G. Kerr in 1898.

Design:This study is a randomized, controlled trial. Participants with a Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition (DSM-IV) diagnosis of bipolar I disorder, manic or mixed episode will be randomly assigned to a treatment of Lithium, Valproate, Oxcarbazepine, Quetiapine, Olanzapine, or Ziprasidone. In the following conditions, participants will take another antimanic drug as a combination medication: 1) those who have a reduction in YMRS scores less than 25% after one week of treatment; 2) those who have a reduction in YMRS scores less than 50% after two weeks of treatment; or 3) those who have a increase in YMRS more than 30% at day 4. An antipsychotic (Quetiapine, Olanzapine, and Ziprasidone) will be added on for those who use lithium, Valproate or Oxcarbazepine as a first attempted medication; while Lithium, Valproate, or Oxcarbazepine will be added on for those who use an antipsychotic as a first attempted medication. Those participants who are recognized as non-response/partial response to two combined medications after 6 weeks of treatment will switch to Modified Electroconvulsive Therapy (MECT).

Measures: Primary outcome measures are change scores on the Young Mania Rating Scale (YMRS) and dropout rates. Secondary outcome measures include Clinical Global Impressions (CGI) Scale, Global Assessment Scale (GAS), Treatment Emergent Symptom Scale (TESS), and Brief Psychiatric Rating Scale (BPRS).

Response criteria: <25% reduction in YMRS scores or >=4 scores of CGI is defined as non-response. 25-49% reduction in YMRS scores from baseline as well as <=3 scores of Clinical General Impression (CGI) is recognized as partial response.>= 50% reduction in YMRS as well as 1 (very much improved) or 2 scores (much improved) of CGI is recognized as response. Remission is defined as a YMRS score <=12 and CGI score equal to 1 or 2.

Detailed Description

Background:

Bipolar disorder is one of the most common mental illnesses affecting 1%-4% of the population, and one of the leading causes of worldwide disability. Mania is a condition of excessively elevated mood, characterizes bipolar disorder, and usually is a main cause of hospitalization. Mood stabilisers and antipsychotic drugs have long been the maintenance treatment of acute mania with and without psychotic symptoms. Though clinical trails have been demonstrated that these drugs are individually more effective than placebo.However, in the pragmatic practice, patient at acute mania urgently want to see the effectiveness, and psychiatrist under great pressure and are in great need to evaluate the very short-term effectiveness (e.g one week). If the first attempted antimanic drug fails, psychiatrist need the evidence that which medication should be to added on or switch to.

Objectives:

one main aim is to rank the short-term ( e.g.one and two week) effectiveness and acceptability of the common anti-mania drugs, including Lithium, Valproate, Oxcarbazepine, Quetiapine, Olanzapine, or Ziprasidone. Secondary aim is to investigate which medication to add on for non-responders or switch to.

Methods:

The study setting: it is expected that 120 subjects with a diagnose of DSM-IV bipolar disorder will be recruited from Guangzhou Psychiatric Hospital, the earliest psychiatric hospital in the history of China established by Dr.J. G. Kerr in 1898.

Design:This study is a randomized, controlled trial, consisting two phase. 120 participants with a Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition (DSM-IV) diagnosis of bipolar I disorder, manic or mixed phase will be randomly assigned to a treatment of Lithium, Valproate, Oxcarbazepine, Quetiapine, Olanzapine, or Ziprasidone. The period from starting dose to effective dose for each drug is within 2 days, and the effective doses for these drugs are described as follow: Lithium, 750mg-2000mg/d, serum Li level: 0.6mmol-1.2mmol/L; Valproate, 800mg-- 1200mg/d, serum Valproate level: 70-120ug/ml; Oxcarbazepine, 600-1200mg/d; Quetiapine, 600mg--800mg/d; Olanzapine, 10mg-- 20mg/d; Ziprasidone, 80mg-160mmg/d.

In the following conditions, participants will take a another antimanic drug as a combination medication: 1) those who have a reduction in YMRS scores less than 25% after one week of treatment; 2) those who have a reduction in YMRS scores less than 50% after two weeks of treatment; or 3) those who have a increase in YMRS more than 30% at day 4. An antipsychotic (Quetiapine, Olanzapine, and Ziprasidone) will be added on for those who use lithium, Valproate or Oxcarbazepine as a first attempted medication; while Lithium, Valproate, or Oxcarbazepine will be added on for those who use an antipsychotic as a first attempted medication. Those participants who are recognized as non-response/partial response to two combined medications after 6 weeks of treatment will switch to Modified Electroconvulsive Therapy (MECT).

Measures: Primary outcome measures are change scores on the Young Mania Rating Scale (YMRS) and dropout rates. Secondary outcome measures include Clinical Global Impressions (CGI) Scale, Global Assessment Scale (GAS), Treatment Emergent Symptom Scale (TESS), and Brief Psychiatric Rating Scale (BPRS).

Response criteria: <25% reduction in YMRS scores or >=4 scores of CGI is defined as non-response. 25-49% reduction in YMRS scores from baseline as well as <=3 scores of Clinical General Impression (CGI) is recognized as partial response.>= 50% reduction in YMRS as well as 1 (very much improved) or 2 scores (much improved) of CGI is recognized as response. Remission is defined as a YMRS score <=12 and CGI score equal to 1 or 2.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
120 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Participant)
Primary Purpose:
Treatment
Official Title:
Comparative Efficacy and Acceptability of Lithium, Valproate, Oxcarbazepine, Quetiapine, Olanzapine, and Ziprasidone in Bipolar I Disorder, Manic or Mixed Phase
Study Start Date :
Sep 1, 2013
Anticipated Primary Completion Date :
Dec 1, 2015
Anticipated Study Completion Date :
Dec 1, 2015

Arms and Interventions

Arm Intervention/Treatment
Experimental: Valproate

Name: Valproate; dosage form: tablet, 250mg; dosage and frequency: 800mg-- 1200mg/d; duration: 6 weeks.

Drug: Valproate
Valproate is used as a mood stabiliser
Other Names:
  • Depakote
  • Experimental: Oxcarbazepine

    Name: Oxcarbazepine, dosage form: 300mg, tablet; dosage and frequency: 600-1200mg/d; duration: 6 weeks

    Drug: Oxcarbazepine
    Oxcarbazepine is used as a mood stabiliser
    Other Names:
  • Trileptal
  • Experimental: Quetiapine

    name: Quetiapine, dosage form: 200mg,tablet; dosage and frequency: 600mg-- 800mg/d; duration: 6 weeks

    Drug: Quetiapine
    Quetiapine is used as a mood stabiliser
    Other Names:
  • SEROquel
  • Experimental: Olanzapine

    Name: Olanzapine, dosage form: 5mg tablet; dosage and frequency: 10mg--20mg/d; duration: 6 weeks

    Drug: Olanzapine
    Olanzapine is used as a mood stabiliser.
    Other Names:
  • Zyprexaï¼›
  • Experimental: Ziprasidone

    Name: Ziprasidone, dosage form: 10mg tablet; dosage and frequency: 80mg-160mmg/d; duration: 6 weeks

    Drug: Ziprasidone
    Ziprasidone is used as a mood stabiliser
    Other Names:
  • Geodon
  • Experimental: Lithium

    name: lithium; dosage form: 250mg Tablet; dosage and frequency: 750mg-2000mg/d;serum Li level: 0.6mmol-1.2mmol/L; duration: 6 weeks

    Drug: Lithium
    Lithium is used as a mood stabiliser
    Other Names:
  • lithium Carbonate
  • Outcome Measures

    Primary Outcome Measures

    1. Change from baseline in Young Mania Rating Scale at 2 weeks and 6 weeks [Baseline, 2 weeks and 6 weeks]

      Young Mania Rating Scale is used to assess hypomania/mania symptoms

    2. rate of dropout (treatment discontinuation) [1,2,4,6 weeks]

      to compare the rates of treatment discontinuation of different drugs because of side effect or effectiveness

    Secondary Outcome Measures

    1. Clinical Global Impressions (CGI) Scale [baseline, 2 weeks, 4 weeks, and 6 weeks]

      Clinical Global Impressions (CGI) Scale is used to assess the patient's global functioning prior to and after initiating a study medication. The CGI provides an overall clinician-determined summary measure, taking into account all available information, including a knowledge of the patient's history, psychosocial circumstances, symptoms, behavior, and the impact of the symptoms on the patient's ability to function

    2. Brief Psychiatric Rating Scale [baseline, 2, 3, 4 and 6 weeks]

      Brief Psychiatric Rating Scale is used to assess psychotic symptoms.

    3. Global Assessment Scale [baseline, 2, 3, 4 and 6 weeks]

      Global Assessment Scale is a numeric scale (1 through 100) used by mental health clinicians to rate the general functioning.

    4. Treatment Emergent Symptom Scale [2, 3, 4 and 6 weeks]

      Treatment Emergent Symptom Scale is used to assess the adverse event of the drug.

    5. Hamilton Anxiety Rating Scale [baseline, 2, 3, 4, and 6 weeks]

      Hamilton Anxiety Rating Scale is used to assess anxious symptoms

    6. Hamilton Depression Rating Scale [baseline, 2, 3, 4, and 6 weeks]

      Hamilton Depression Rating Scale is used to assess the depressive symptoms

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 65 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • with a diagnosis of bipolar I disorder, manic or mixed phase

    • equal or more than 18 scores in Young Mania Rating Scale (YMRS)

    Exclusion Criteria:
    • Serious general medical illness

    • pregnancy and lactation

    • given long-acting antipsychotic drug within the last two month

    • endocrine disease( e.g.Diabetes and thyrotoxicosis)

    • given thyroxine therapy within the last three months or is being given hormone therapy

    • sexually active and not using contraceptives

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Guangzhou Psychiatric Hospital Guangzhou Guangdong China 510370
    2 Guangzhou Psychiatric Hospital Guangzhou Guangdong China 510370

    Sponsors and Collaborators

    • Guiyun Xu
    • The University of Hong Kong

    Investigators

    • Principal Investigator: Guinyun Xu, M.D, Guangzhou Psychiatric Hospital
    • Principal Investigator: Kangguang Lin, M.D, The University of Hong Kong

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    Guiyun Xu, Associate Professor, Guangzhou Psychiatric Hospital
    ClinicalTrials.gov Identifier:
    NCT01893229
    Other Study ID Numbers:
    • 20120509
    First Posted:
    Jul 8, 2013
    Last Update Posted:
    Mar 17, 2015
    Last Verified:
    Mar 1, 2015
    Keywords provided by Guiyun Xu, Associate Professor, Guangzhou Psychiatric Hospital
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Mar 17, 2015