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临床试验/NCT01240096
NCT01240096已完成4 期

Phase 4 Study of Mirtazapine in Functional Dyspepsia Patients With Weight Loss

Universitaire Ziekenhuizen KU Leuven1 个研究点 分布在 1 个国家目标入组 35 人开始时间: 2006年9月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
已完成
入组人数
35
试验地点
1
主要终点
Difference in dyspepsia symptom scores week 8 versus week 0

研究概览

简要总结

Double-blind randomized controlled trials of 8 weeks mirtazapine 15 mg daily or placebo, followed by 8 weeks of open-label mirtazapine 15 mg daily

详细描述

Double-blind randomized controlled trials of 8 weeks mirtazapine 15 mg or placebo, followed by 8 weeks of open-label mirtazapine

Two weeks run-in, 8 weeks randomized, 8 weeks open label

Assessments include

  • dyspepsia questionnaire
  • Nepean dyspepsia index
  • Daily diary
  • Vital signs

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
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Functional dyspepsia according to Rome II criteria
  • Weight loss of > 5% body weights

排除标准

  • Organic GI pathology
  • History of upper gi tract surgery
  • Major depression or anxiety
  • Use of antidepressants in the last 2 months
  • Prokinetic drugs or spasmolytic drugs
  • Analgesic use (except paracetamol)
  • Pregnancy or lactation

研究组 & 干预措施

Mirtazapine

Active Comparator

mirtazapine 15 mg daily

干预措施: Mirtazapine (Drug)

Placebo

Placebo Comparator

Placebo once daily

干预措施: Mirtazapine (Drug)

结局指标

主要结局

Difference in dyspepsia symptom scores week 8 versus week 0

时间窗: Week 8 compared to week 0

The Dyspepsia Symptom Score is calculated from the dyspepsia symptom severity questionnaire at weeks 0, 4 and 8. The symptom score has been used in previous studies (Tack et al., Gastroenterology 1998).

次要结局

  • Individual symptom severities(Week 8 compared to week 0)
  • Nepean dyspepsia index for quality of life in functional dyspepsia(Week 8 compared to week 0)

研究者

申办方类型
Other

研究点 (1)

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