Benefits of Switching Antidepressants Following Early Nonresponse
关键词
抽象
描述
To the researchers' knowledge, there is no report to prospectively examine the benefits of switching antidepressants following early nonresponse. In this prospective 24-week study, the researchers will compare clinical outcomes between switching antidepressants and maintaining the same antidepressant in patients with major depressive disorder who do not show a 20% reduction in symptoms at week 2.
Materials and Methods: This open-label 24-week randomized controlled trial will be performed at psychiatric hospitals in Tokyo, Japan.
This study will be conducted with the approval of the Institutional Review Board of each participating hospital, and written informed consent will be obtained from all of the participants after providing a full explanation about the study.
In the short-term acute phase, sertraline will be initiated at 25 mg, increased to 50 mg on day 3, and maintained until day 14. If patients show an early response (i.e. ≧ 20% improvement in the MADRS total score from baseline), sertraline will be continued and titrated at 50 - 100 mg based on clinical judgment. On the other hand, if patients show no early response, they will be randomly divided into two groups. In one group, sertraline will be continued and titrated at 50 - 100 mg, whereas in the other group sertraline will be switched to paroxetine. Paroxetine will be started at 10 mg on days 15 and 16, increased to 20 mg on day 17, and further increased weekly by 10 mg from week 4 (i.e. day 22), while sertraline will be tapered by 25 mg each on days 15 and 16. In case patients are intolerant to adverse events, or they achieve remission (i.e. the MADRS total score ≦ 8), increasing the dose will be terminated. Lorazepam, lormetazepam, and mosapride will be allowed on a p.r.n. basis.
In the long-term follow-up phase after week 8, patients who achieve remission or response will be followed up and the same dose will be administered throughout. Assessments will include the MADRS, the clinical global impression scale (CGI), and the Quick Inventory of Depressive Symptomatology self-reported (QIDS-SR) (weeks 1, 2, 3, 4, 6, 8, 12, 16, 20, and 24). Adverse events will also be monitored on every visit.
日期
| 最后验证: | 08/31/2009 |
| 首次提交: | 08/19/2007 |
| 提交的预估入学人数: | 08/19/2007 |
| 首次发布: | 08/20/2007 |
| 上次提交的更新: | 09/25/2009 |
| 最近更新发布: | 09/27/2009 |
| 实际学习开始日期: | 07/31/2007 |
| 预计主要完成日期: | 11/30/2010 |
| 预计完成日期: | 11/30/2010 |
状况或疾病
干预/治疗
Drug: Arm-1
Drug: 2
相
手臂组
| 臂 | 干预/治疗 |
|---|---|
| Active Comparator: Arm-1 Sertraline to Paroxetine | Drug: Arm-1 For subjects enrolled in this arm, sertraline will be initiated at 25mg, increased to 50mg on day 3, and maintained until day 14. If subjects show an early response (i.e. a 20% improvement in the MADRS total score from baseline) at week 2, sertraline will be continued and titrated at 50 - 100mg based on clinical judgment. On the other hand, if subjects fail to show an early response at week 2, they will be randomly divided into two groups. In one group, sertraline will be continued and titrated at 50 - 100mg, whereas in the other group sertraline will be switched to paroxetine. In this switching group, paroxetine will be started at 10mg on days 15 and 16, increased to 20mg on day 17, and further increased to 40mg by a weekly 10mg increase, while sertraline will be dosed at 25mg on day 15 and terminated on day 16. |
| Active Comparator: 2 Paroxetine to Sertraline | Drug: 2 Paroxetine will be initiated at 10mg, increased to 20mg on day 3, and maintained until day 14. If subjects show an early response (i.e. a 20% improvement in the MADRS total score from baseline) at week 2, paroxetine will be continued and titrated at 20 - 40mg based on clinical judgment. On the other hand, if subjects fail to show an early response at week 2, they will be randomly divided into two groups. In one group, paroxetine will be continued and titrated at 20 - 40mg, whereas in the other group paroxetine will be switched to sertraline. In this switching group, sertraline will be started at 25mg on days 15 and 16, increased to 50mg on day 17, and further increased to 100mg by a weekly 25mg increase, while paroxetine will be dosed at 10mg on day 15 and terminated on day 16. |
资格标准
| 有资格学习的性别 | All |
| 接受健康志愿者 | 是 |
| 标准 | Inclusion Criteria: 1. Inpatients and outpatients who meet the Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition (DSM-IV) criteria of major depression disorder (MDD) 2. Have not taken antidepressants for the previous one month 3. Do not have emergent suicidal ideation defined as a score of 4 or less on suicidal thoughts item in the MADRS. Exclusion Criteria 1. Unstable physical illness or clinically significant neurological disorder 2. Having emergent suicidal idea defined as a score of 5 or more on the suicidal thoughts item in the MADRS. 3. Having history of non-response or intolerance to paroxetine or sertraline. This study will be conducted with the approval of the Institutional Review Board of each participating hospital, and written informed consent will be obtained from all of the participants after providing a full explanation of the study. |
结果
主要结果指标
1. The Montgomery-Asberg Depression Rating Scale [at weeks1, 2, 3, 4, 6, 8, 12, 16, 20, 24 and 48 - 52.]
次要成果指标
1. The Clinical Global Impression 2. The Quick Inventory of Depressive Symptomatology self-reported [at weeks1, 2, 3, 4, 6, 8, 12, 16, 20, 24 and 48 - 52.]
