NL-OMON54182尚未招募3 期
Sodium-oxybate as a potential new treatment for catatonia in patients with depression, bipolar disorder or a psychotic disorder, a randomized controlled trial. The Laborit study. - Laborit study
Amsterdam UMC0 个研究点目标入组 42 人开始时间: 待定最近更新:
适应症
试验速览
- 阶段
- 3 期
- 状态
- 尚未招募
- 发起方
- 入组人数
- 42
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 18 至 99（—）
入选标准
- •-Patients (age 18-80) with catatonia
- •-With DSM-5 diagnosis of either unipolar depression, bipolar disorder, or a
- •psychotic disorder admitted to an acute psychiatric ward.
- •-No response to usual care, with increasing doses of lorazepam to a maximum of
- •24 mg during 4 days.
- •-Presence of catatonia will be assessed using the BFCTRS(15). Catatonia is
- •considered present with a score of two or higher on the BFCTRS.
- •-Catatonia is present for a maximum of eight weeks.
排除标准
- •-Somatic disorder underlying catatonia.
- •-Use of anti-psychotic drugs.
- •-Known heart failure or renal impairment due to signifcant amounts of sodium in
- •the sodium-oxybate.
- •-Known sleep apnea.
- •-Use of Gabaergic drugs including gabapentin or pregabalin or clonidine. Or us
- •of valproate.
- •-Presence of alcohol use disorder
- •-Presence of malignant catatonia or development of catatonia during the study,
- •i.e. those with malignant catatonia will be treated immediately with ECT
研究者
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