NCT Number: NCT00209963
A Study of Gaboxadol in Primary Insomnia
To evaluate the safety and tolerability of gaboxadol in primary insomnia.
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Notify MeKey information
Conditions
Age range
18 year–65 year
Sex eligibility
All sexes
Study type
Interventional
Phase
Phase 3
About this study
To obtain long-term safety and tolerability data with gaboxadol.
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- patients with Primary insomnia
Treatment and study plan
Primary outcomes
-
Long-term safety in gaboxadol.
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
- 2003
- 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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