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Sleep Inducing And Maintaining Efficacy Of Circadin In Elderly Insomniacs (Neu I)

Primary Purpose

Primary Insomnia

Status
Completed
Phase
Phase 2
Locations
France
Study Type
Interventional
Intervention
placebo Circadin
Circadin
Sponsored by
Neurim Pharmaceuticals Ltd.
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Primary Insomnia focused on measuring Insomnia, Primary insomnia, sleep latency, non restorative sleep, sleep quality, Double-Blind, Placebo Controlled, Parallel-Group, Sleep Laboratory Study

Eligibility Criteria

55 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Healthy male and female, aged ≥ 55 years, suffering from primary insomnia according to DSM-IV criteria (307.42)

Exclusion Criteria:

  • According to DSM-IV, subjects belonging to the following groups are excluded: 780.59; 307.45; 307.47; 780.xx (Appendix 2);
  • Use of benzodiazepines or other hypnotics during the preceding 1 month with a frequency of more than 2 times a week and lasting more than 2 weeks;
  • Severe neurological, psychiatric or sleep disorders;
  • Other serious diseases;
  • Taking more than 1/2 l of alcohol, more than 3 cups of coffee or more than 10 cigarettes per day .
  • Subjects who need beta blockers as a treatment.

Sites / Locations

  • FORENAP

Arms of the Study

Arm 1

Arm 2

Arm Type

Placebo Comparator

Experimental

Arm Label

placebo

Circadin

Arm Description

Outcomes

Primary Outcome Measures

Secondary Outcome Measures

Full Information

First Posted
December 31, 2008
Last Updated
January 4, 2009
Sponsor
Neurim Pharmaceuticals Ltd.
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1. Study Identification

Unique Protocol Identification Number
NCT00816673
Brief Title
Sleep Inducing And Maintaining Efficacy Of Circadin In Elderly Insomniacs
Acronym
Neu I
Official Title
Phase II Study of Sleep Inducing And Maintaining Efficacy Of Circadin In Elderly Insomniacs.
Study Type
Interventional

2. Study Status

Record Verification Date
January 2009
Overall Recruitment Status
Completed
Study Start Date
September 1996 (undefined)
Primary Completion Date
May 1997 (Actual)
Study Completion Date
September 1997 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
Neurim Pharmaceuticals Ltd.

4. Oversight

5. Study Description

Brief Summary
The aim of this placebo controlled study is to investigate the effect of 2 mg melatonin Slow Release (Circadin®) on the sleep/wake cycle in elderly insomniac out-subjects, aged 55 years or more.
Detailed Description
Circadin® is a newly developed slow release galenic formulation of melatonin, producing overall levels of melatonin comparable to those observed in a control population, when administered to patients with deficiency in melatonin; thus it deserves more clinical and paraclinical investigations for establishing efficacy in inducing and maintaining sleep and for safety. Since, on the one hand, the endogenous substance melatonin has beneficial effects on sleep in man and, on the other hand, there is a decrease in melatonin secretion in elderly people, substitution therapy in elderly insomniacs would be a desirable therapy. The aim of this placebo controlled study was to investigate the effect of 2 mg Melatonin Slow Release (Circadin®) on the sleep/wake cycle in elderly insomniac out-subjects, aged 55 years or more. Sleep was assessed by means of polysomnography (hypnographic results), all-night sleep EEG spectral analysis (functional and quantitative results of sleep EEG), actimetry (SomnitorTM), wake EEG and sleep/wake quality questionnaires. Vigilance and cognitive skills were assessed by means of psychomotor and neurocognitive tests derived from the Leeds psychomotor test battery (vigilance and arousal) and TEA battery (attention).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Primary Insomnia
Keywords
Insomnia, Primary insomnia, sleep latency, non restorative sleep, sleep quality, Double-Blind, Placebo Controlled, Parallel-Group, Sleep Laboratory Study

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
40 (Actual)

8. Arms, Groups, and Interventions

Arm Title
placebo
Arm Type
Placebo Comparator
Arm Title
Circadin
Arm Type
Experimental
Intervention Type
Drug
Intervention Name(s)
placebo Circadin
Intervention Description
Placebo tabs of Prolonged release melatonin
Intervention Type
Drug
Intervention Name(s)
Circadin
Other Intervention Name(s)
ATC code: N05CH01
Intervention Description
prolonged release melatonin 2 mg taken daily 2 hours before bed-time for 3 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
55 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Healthy male and female, aged ≥ 55 years, suffering from primary insomnia according to DSM-IV criteria (307.42) Exclusion Criteria: According to DSM-IV, subjects belonging to the following groups are excluded: 780.59; 307.45; 307.47; 780.xx (Appendix 2); Use of benzodiazepines or other hypnotics during the preceding 1 month with a frequency of more than 2 times a week and lasting more than 2 weeks; Severe neurological, psychiatric or sleep disorders; Other serious diseases; Taking more than 1/2 l of alcohol, more than 3 cups of coffee or more than 10 cigarettes per day . Subjects who need beta blockers as a treatment.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jean Paul MACHER, MD
Organizational Affiliation
Forenap
Official's Role
Principal Investigator
Facility Information:
Facility Name
FORENAP
City
Centre Hospitalier de Rouffach
ZIP/Postal Code
F-68250
Country
France

12. IPD Sharing Statement

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Sleep Inducing And Maintaining Efficacy Of Circadin In Elderly Insomniacs

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