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 a 40-week Period

CompletadoFase 3ClinicalTrials.gov

ID: NCT00253903Tipo: INTERVENTIONALInicio: 1 de nov de 2005Fin estimado: 1 de sept de 2008

Traducción no disponible, mostrando original

Resumen

The purpose of the study is to assess efficacy and safety of eplivanserin in the population of patients complaining of sleep maintenance insomnia. The patients suffering from that condition frequently wake up during the night, their sleep is nonrestorative and they suffer from a significant distress or impairment in their daily activities consecutive to insomnia.

Descripción detallada

The study is being conducted worldwide. It consists of 4 segments: * Segment A: 7-day run-in (screening) * Segment B: 12-week double blind treatment * Segment C: 40-week open treatment extension * Segment D: 2-week run-out period

Elegibilidad

Edad mínima: 18 YearsSexo: ALL

Criterios de inclusión

Out patients
Each patient must have primary insomnia in accordance with DSM-IV-TR-Axis I criteria
Based on patient's information, the patient has spent at least 6.5 hours and not more than 9.0 hours, in bed, each night, over the preceding two weeks.
Based on patient's information, the 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 visit and randomization visit.

Criterios de exclusión

Females who are lactating or pregnant
Woman of childbearing potential with a positive serum beta human chorionic gonadotropin pregnancy test at screening and not using an acceptable form of contraception
Patients presenting with acute or chronic pain resulting in insomnia
Patients with history of epilepsy or seizures
Consumption of xanthine containing beverage (i.e. tea, coffee, or cola) comprising more than 5 glasses/day
Evidence of any clinically significant, severe, or unstable acute or chronically progressive medical or surgical disorder which may affect patient safety
BMI \>32
Acute or chronic pain resulting in insomnia
Patients with current psychiatric disorders according to DSM-IV-TR criteria, mental retardation, or dementia
Clinically significant and abnormal EKG (QTc interval \>500 msec)
Positive for hepatitis B or C
Serious head injury or stroke within 1 year
Use of OTC medications such as valerian root, kava, melatonin, St. John's Wort, or alluna; prescription sleep medications or anxiolytics within 1 week or 5 half-lives
Participation in another trial within two month before the screening visit
Use of any substance with psychotropic effects or properties known to affect sleep/wake
Unable to complete the study questionnaires
Night shift workers, and individuals who nap 3 or more times per week over the preceding month
History of:
Primary hypersomnia
Narcolepsy
Breathing-related sleep disorder (such as sleep apnea)
Circadian rhythm sleep disorder
Parasomnia (somnambulism)
Dyssomnia (such as periodic leg movements)

Intervenciones

drug

eplivanserin (SR46349)

oral administration

drug

placebo

oral administration

Ubicaciones

Sanofi-Aventis Administrative Office

Buenos Aires, Argentina

Patrocinadores

PrincipalSanofi

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