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临床试验/EUCTR2005-003082-16-CZ
EUCTR2005-003082-16-CZ进行中(未招募)不适用

Efficacy and safety of eplivanserin 5mg/day on Sleep Maintenance Insomnia : a 12-week multicenter, randomized, double-blind, placebo-controlled study followed by an open treatment phase extension with eplivanserin for 40 weeks period - EPLILONG

Sanofi-aventis recherche et développement0 个研究点目标入组 1,120 人开始时间: 2005年11月7日最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
1,120

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

性别
All

入选标准

  • - Out-patients aged =18 years.
  • - Diagnosis of primary insomnia based on criteria (DSM-IV-TR) with predominant complaints of difficulty in initiating or maintaining sleep (nocturnal awakenings), or nonrestorative sleep for at least one month preceding the study visit.
  • (1) Disturbances of sleep maintenance:Based on patient’ s information:
  • - Patient has spent at least 6.5 hours and no more than 9.0 hours, in bed, each night, over the preceding two weeks.
  • -Patient must complain of at least one hour of wakefulness after sleep onset for at least 3 nights per week over the preceding month.
  • - Patient must report impact daytime functioning associated with sleep maintenance insomnia as measured by question 3 of Insomnia Severity Index at screening and randomization visits.
  • (2) Based on the information recorded in the patient’s diary during the screening week preceding the randomization the following criteria must be present:
  • a) Mean WASO per night = 60mn during screening period (7 days) and no period of WASO < 45mn on each screening night,
  • b)TST < 7 hours and > 3 hours on 3-worst screening nights.
  • c) Mean SOL during the screening period have to be = 30mn.
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • 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

排除标准

  • - Females who are lactating or who are pregnant,
  • - Woman of childbearing potential with a positive serum beta-human chorionic gonadotropin (bHCG) pregnancy test at screening and not using an acceptable form of contraception,
  • - Patients presenting with acute or chronic pain resulting in insomnia,
  • - Patients with current psychiatric disturbances
  • - Patients with a history of epilepsy or seizures, with clinically significant, severe or unstable, acute or chronically progressive medical or surgical disorder, with history of serious head injury or stroke
  • - Patients with clinically significant and abnormal ECG
  • - Use of any prescription or OTC sleep medication
  • - Use of substances with psychotropic effects or porperties known to affect sleep/awake
  • - Night shift workers, and individuals who nap 3 or more times per week over the preceding month,
  • - History of (i) primary hypersomnia, (ii) narcolepsy, (iii) breathing-related sleep disorder, (iv) circadian rhythm sleep disorder, (v) parasomnia (e.g. somnambulism), (vi) dyssomnia not otherwise specified, i.e. periodic leg movement syndrome.

研究者

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