跳至主要内容
临床试验/NCT02726659
NCT02726659终止3 期

Adjunctive Use of Celecoxib in the Treatment of Bipolar Postpartum Depression: a Randomized, Double-blind, Placebo-controlled Trial

Lawson Health Research Institute1 个研究点 分布在 1 个国家目标入组 1 人开始时间: 2016年5月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
3 期
状态
终止
入组人数
1
试验地点
1
主要终点
Hamilton Rating Scale for Depression (HAM-D)

研究概览

简要总结

The investigators will conduct a 6-week, randomized, double-blind, placebo-controlled trial of celecoxib as an add-on treatment to the mood stabilizer among women with bipolar I or II postpartum depression. Women who are taking a mood stabilizer for treatment of bipolar disorder in the postpartum treatment will receive either a placebo or celecoxib add-on treatment. Patients will be monitored regularly to assess psychiatric symptoms and side effects. The investigators aim to evaluate the potential antidepressant effect of celecoxib in bipolar postpartum depression.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Triple (Participant, Care Provider, Investigator)

入排标准

年龄范围
18 Years 至 45 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • women aged 18-45 who are within 3 months of delivering a healthy, term (37 to 40 weeks) singleton
  • diagnosis of bipolar postpartum depression - depressed with peripartum onset
  • have a 17-item Hamilton Rating Scale for Depression score of >18
  • have failed to respond to an adequate trial of the mood stabilizer
  • are currently not on any psychotropic drug except a mood stabilizer (lithium, lamotrigine or quetiapine)
  • are able to communicate (written and oral) in English and capable of giving consent

排除标准

  • current major depressive episode of more than 6 months duration
  • a current comorbid psychiatric disorder
  • history of alcohol or substance abuse within the 12 months before screening
  • concurrent psychotherapy
  • high risk for suicide (actively suicidal or a score of = 3 on item #3 on HAM-D)
  • current hepatic, renal, or cardiac disease, chronic pain, coagulation disorders, esophageal or gastro duodenal ulceration within the previous 30 days
  • known immediate-type hypersensitivity to COX-2 inhibitors, sulfonamides, ibuprofen, or diclofenac
  • breastfeeding mothers

研究组 & 干预措施

Celecoxib

Experimental

Adjunct celecoxib in 6 week treatment

干预措施: Celecoxib (Drug)

Placebo

Placebo Comparator

Adjunct placebo in 6 week treatment

干预措施: Placebo (Drug)

结局指标

主要结局

Hamilton Rating Scale for Depression (HAM-D)

时间窗: 6 weeks

To assess the effectiveness of the addition of celecoxib in the treatment of bipolar postpartum depression by the change in mean scores on the HAM-D between baseline and the 6 weeks endpoint. Response will be a \> 50% reduction in HAM-D score and remission will be a \< 7 HAM-D score from baseline to week 6.

次要结局

  • Edinburgh Postnatal Depression Scale (EPDS)(6 weeks)
  • Montgomery Asberg Depression Scale(6 weeks)
  • Udvalg for Kliniske Undersogelser Scale(6 weeks)
  • Clinical Global Impression Scale (CGI)(6 weeks)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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