EUCTR2017-004514-25-ES进行中(未招募)1 期
EFFICACY AND SAFETY OF THE ADMINISTRATION OF THE PASSIFLORA EXTRACT FOR BENZODIAZEPINE WITHDRAWAL IN INSTITUTIONALIZED OLDER ADULTS : CLINICAL TRIAL PHASE III. - SEDISTRESS
utrición Medica S.L.0 个研究点目标入组 108 人开始时间: 2018年6月20日最近更新:
适应症
相关药物
试验速览
- 阶段
- 1 期
- 状态
- 进行中(未招募)
- 发起方
- 入组人数
- 108
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional clinical trial of medicinal product
入排标准
入选标准
- •1. Age > 65 years old
- •2. Stable dose of benzodiazepines during last 3 months ( 4mg loracepam per day or equivalent)
- •3. Capable of giving consent and to answer the questionnaires according to researcher criteria
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) no
- •F.1.2.1 Number of subjects for this age range
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range 108
排除标准
- •1. Diagnosis of dementia moderate or severe (Test Minimental = 20).
- •2. Acute confusional syndrome at the inclusion
- •3- Panic disorder
- •4. Obsesive-compulsive disorder
- •5. Any type of psycosis or bipolar disorder
- •6. Severe Parkison disease diagnosed
- •7. Current or past diagnosis of epilepsia
- •8. Recent stroke (last month)
- •9. Thyroid disorders not controlled or uncompensated
- •10. Alteration of deglutition
- •11. Previous drugs or alcohol abuse
- •12. Hospitalization (more than 24 hours) during the last month
- •13. Complex priority treatment (dialisis, chemotherapy...)
- •14. Life expectation less than 1 year
- •15. Benzodiazepines therapeutic uses not for anxiety or insomnio
研究者
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