跳至主要内容
临床试验/EUCTR2017-000990-35-IT
EUCTR2017-000990-35-IT进行中(未招募)1 期

EFFECTS OF ANTIDEPRESSANT TREATMENT WITH AGOMELATINE ON PATIENTS AFFECTED BY DEPRESSION AND EPILEPSY. A DOUBLE BLIND RANDOMIZED STUDY WITH ACTIVE CONTROL (ESCITALOPRAM) WITH PARALLEL GROUPS. - DeprEpil

DIP. MEDICINA DEI SISTEMI UNIVERSITà DEGLI STUDI DI ROMA TOR VERGATA0 个研究点目标入组 208 人开始时间: 2020年1月14日最近更新:
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
208

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.Definite diagnosis of epilepsy and antiepileptic medication for more than 6 months;
  • 2.Age 40-75;
  • 3.Beck Depression Inventory –II score >14
  • 4.No previous utilization of any antidepressant agent;
  • 5.Able to co-operate and understand written and oral information;
  • 6.Signed written informed consent.
  • Are the trial subjects under 18? no
  • Number of subjects for this age range: 1
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range 134
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 88

排除标准

  • 1.Patients with hypersensitivity to the Agomelatine and/or Escitalopram;
  • 2.Psychiatric disorders other than depression;
  • 3.Participation in other clinical trials within the last six months prior to inclusion in the present study;
  • 4.Unable to take part in the study as a whole;
  • 5.Use of drugs interfering with CNS other than AEDs;
  • 6.History of pseudoseizures, status epilepticus during the previous year;
  • 7.Alterations of blood tests that might interfere with the participation and/or completion of the study by the patient;
  • 8.Patients with hepatic injury, or with transaminases levels three times the upper limit of normal (ULN), or hepatic risk factors such as obesity/overweight/non-alcoholic fatty liver disease, diabetes, substantial alcohol intake or concomitant medicinal products associated with risk of hepatic injury.
  • 9.Concomitant treatment based on strong CYP1A2 inhibitors;
  • 10.Women of childbearing potential who are not using effective contraception;
  • 11.Women with suspected or confirmed pregnancy and breastfeeding;
  • 12.Concomitant hormonal therapy;
  • 13.QTc interval>450 msec.

研究者

发起方
DIP. MEDICINA DEI SISTEMI UNIVERSITà DEGLI STUDI DI ROMA TOR VERGATA

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