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OpenTrials
Completed

NCT Number: NCT00209924

A Study of Gaboxadol in Primary Insomnia

To evaluate the efficacy safety and tolerability of gaboxadol in primary insomnia.

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Key information

Conditions

Primary Insomnia Dyssomnias Mental Disorders Nervous System Diseases Sleep Disorders, Intrinsic Sleep Initiation and Maintenance Disorders Sleep Wake Disorders

Age range

66 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 3

Primary location

Non-US study, principal location:

Gothenburg, Sweden

About this study

To compare hypnotic efficacy of gaboxadol with placebo in elderly outpatients with primary insomnia

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • patients with a diagnosis of primary insomnia

Treatment and study plan

Gaboxadol

Drug

Primary outcomes

  1. Efficacy

  2. Safety

  3. Tolerability

Sponsors and collaborators

Lead sponsor

H. Lundbeck A/S

Industry

Registry information

Official study title

A Prospective Randomised Double-Blind Parallel-Group Placebo-Controlled Study of Gaboxadol in Primary Insomnia

Important dates

Study start
2004
Study completion
2005
First posted
Sep 21, 2005
Registry last updated
Mar 30, 2007

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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