Insomnia Clinical Trial
Official title:
A Double-Blind, Randomized, Placebo-Controlled, Multi-Center Dose-Titration Study on the Efficacy and Safety of CHI-921 on Sleep Initiation and Maintenance in Subjects With Insomnia
Insomnia is a disorder where people are having trouble sleeping and can include difficulty falling asleep, staying asleep and waking up too early, as well as having unrefreshing sleep. CHI-921 is a cannabis extract in sunflower oil produced as a treatment for insomnia. This trial is designed to evaluate the efficacy and safety of CHI-921 on people with insomnia.
The study is designed to:
1. Evaluate the patient-reported sleep latency and patient-reported wake after sleep onset
after 3 weeks per treatment dose with CHI-921 compared to placebo.
2. To evaluate the effects of CHI-921 compared to placebo on PSG sleep architecture.
3. To evaluate the effects of CHI-921 compared to placebo on Patient Global Impression of
change.
4. To evaluate the daytime residual effects that may be associated with CHI-921 as compared
to placebo during the double-blind treatment period using patient's morning and evening
questionnaire, Clinical Global Impression of change, Insomnia Severity Index, Pittsburgh
Sleep Quality Index, Epworth Sleepiness Scale as well as the Rey Auditory Verbal
Learning Test and Digit Symbol Substitution psychometric tests.
5. To assess the effect on sleep of abruptly discontinuing CHI-921 compared to placebo
(during run-out period).
6. To evaluate the clinical safety and tolerability of CHI-921 compared to placebo.
7. Evaluation of the accuracy of sleep data obtained by actigraphy as compared to
traditional PSG.
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