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临床试验/NCT06184581
NCT06184581
招募中
4 期

Lithium Versus Lamotrigine in Bipolar Disorder, Type II - a Single Blinded Randomized Controlled Trial (the LiLa-Bipolar RCT)

University Hospital Bispebjerg and Frederiksberg1 个研究点 分布在 1 个国家目标入组 200 人2024年5月8日

概览

阶段
4 期
干预措施
Lithium Carbonate
疾病 / 适应症
Bipolar II Disorder
发起方
University Hospital Bispebjerg and Frederiksberg
入组人数
200
试验地点
1
主要终点
Mood stabilization
状态
招募中
最后更新
上个月

概览

简要总结

The investigators want in a 6-month randomized controlled trial (RCT) to compare effects of lithium versus lamotrigine on mood stabilization and other critical patient outcomes in patients with BDII.

详细描述

Although BDII is more prevalent and with a higher disease burden, including more and longer depressive episodes and lower functioning, than bipolar disorder, type I (BDI), effects of pharmacological treatment including the most frequently used drugs in clinical practice lithium and lamotrigine, is substantially understudied. The investigators want in a 6-month randomized controlled trial (RCT) to compare effects of lithium versus lamotrigine on mood stabilization and other critical patient outcomes in patients with BDII.

注册库
clinicaltrials.gov
开始日期
2024年5月8日
结束日期
2027年12月1日
最后更新
上个月
研究类型
Interventional
研究设计
Parallel
性别
All

研究者

发起方
University Hospital Bispebjerg and Frederiksberg
责任方
Principal Investigator
主要研究者

Lars Vedel Kessing

professor, MD, DMSc.

University Hospital Bispebjerg and Frederiksberg

入排标准

入选标准

  • Bipolar disorder, type II with diagnosis confirmed by SCAN interview
  • Age 18-70 years
  • Habile (i.e., able to give informed consent)

排除标准

  • Past non-response or intolerance to lamotrigine or lithium with \> 6 weeks treatment at an adequate dosage
  • Currently taking mood stabilizers at enrollment in CADIC
  • Severe chronic kidney disease
  • Severe cardiac insufficiency
  • Brugadas syndrome
  • Severe hypothyroidism despite treatment
  • Women who are pregnant, breastfeeding or planning pregnancy in near future.

研究组 & 干预措施

Lithium

tablet

干预措施: Lithium Carbonate

Lamotrigine

tablet

干预措施: Lamotrigine

结局指标

主要结局

Mood stabilization

时间窗: 6 (possibility of 12) months follow-up

Mood Stabilization will be measured by a mood instability score reflecting the daily variability in self-monitored mood collected via the Monsenso app. Patients score their daily mood on a 9-point scale (-3 to +3); scores between -0.5 to 0.5 reflect normal variations, whereas scores of +1, +2 or +3 correspond to mildly, moderately, and severely increased mood and scores of -1, -2 or -3 correspond to mildly, moderately, and severely decreased mood. According to our established methodology, for each participant, we will estimate a mood instability score. Estimates of instability will be based on reading obtained via the Monsenso system which will prompt patients to complete daily mood ratings.

次要结局

  • Non-response(6 (possibility of 12) months follow-up)
  • Depression(6 months)

研究点 (1)

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