Magnetoencephalographic (MEG) Localization of Ramelteon's Effects on Brain Function and Cortical Arousal in Insomnia
Completed
Conditions studied: Insomnia
In brief
The present protocol will utilize simultaneous recording of brain activity during attention and memory tasks in insomnia participants after ramelteon vs. zolpidem vs. placebo administration. The investigators hypothesize that amplitudes of associated with memory will be unchanged by ramelteon, whereas zolpidem will significantly reduce brain activity associated with stimulus processing as evidenced by abnormal reduction in the amplitude of specific brain regions relative to placebo.
Key facts
- Study ID
- NCT00688025
- Run by
- Henry Ford Health System
- People needed
- 24
- Starts
- 2008-05-01
- Expected to finish
- 2010-03-01
- Last updated by the study team
- 2010-03-31
Who can join
Age: 18 and older, up to 55. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Healthy individuals with no secondary condition to insomnia.
You may not qualify if…
- Healthy individuals with no insomnia.
Where it is running
- Henry Ford Hospital Sleep Disorders & Research Center — Detroit, Michigan, United States
Full record on ClinicalTrials.gov
Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.