Study on the preventive effect of ramelteon on the onset of sleep disorder after general anesthesia in patients with autism spectrum disorder: A study protocol.
Study Goal
The researchers aimed to determine whether prophylactic administration of the melatonin receptor agonist ramelteon (Rozerem) could prevent postoperative sleep disorders in patients with autism spectrum disorders (ASD) undergoing general anesthesia.
Results Summary
The study investigates the effectiveness of ramelteon in reducing NREM-REM sleep disorders and circadian rhythm disruptions post-general anesthesia in ASD patients, but specific results are not yet provided in the abstract.
Population
Patients with ASD aged 12 years and above undergoing dental treatment under general anesthesia.
Effective Dosage
Not specified in the abstract.
Duration
7 days prior and 7 days postsurgery.
Interactions
None mentioned
| Intervention | Direction | Endpoint | Population | Dosage | Impact | Claim # |
|---|---|---|---|---|---|---|
general anesthesia | decrease | the cycle of normal physiological sleep | postoperative periods after general anesthesia | - | might significantly disturb and suppress | #1 |
general anesthesia | increase | acute sleep disorder | patients with autism spectrum disorders (ASD) with existing circadian rhythm disorder | - | rapidly deteriorate due to | #2 |
ramelteon (Rozerem) | neutral | sleep disorders | patients with sleep disorders | - | is used as a therapeutic drug | #3 |
ramelteon (Rozerem) | decrease | falling asleep | patients with sleep disorders | - | decreasing the difficulty of | #4 |
prophylactic administration of a sleep-inducing substance, a melatonin receptor agonist | decrease | sleep disorder after general anesthesia | patients with ASD | - | is effective against | #5 |
BACKGROUND: The persistent loss of consciousness caused by general anesthesia without the existence of repeated 90-minute cycles of non-REM and REM sleep might significantly disturb and suppress the cycle of normal physiological sleep in postoperative periods after general anesthesia. Patients with autism spectrum disorders (ASD) with existing circadian rhythm disorder are reported to rapidly deteriorate due to acute sleep disorder during the perioperative period after general anesthesia.A melatonin receptor agonist, ramelteon (Rozerem), which is a sleep cycle regulator, is used as a therapeutic drug for patients with sleep disorders, but there are no studies on the prevention of postoperative sleep disorder after general anesthesia.In this study, we investigate whether prophylactic administration of a sleep-inducing substance, a melatonin receptor agonist, is effective against sleep disorder after general anesthesia in patients with ASD. METHODS/DESIGN: This study is intended for patients with ASD aged 12 years and above who undergo treatment at Nagasaki University Hospital, Isahaya General Hospital Dentistry, and Sasebo City General Medical Center Dentistry and undergo dental treatment under general anesthesia. A melatonin receptor agonist (Rozerem) will be taken 7 days prior and 7 days postsurgery in patients diagnosed with insomnia. A randomized comparison will be made between 2 groups: an experimental group that is additionally administered Rozerem and a control group.The primary endpoint is the incidence of NREM-REM sleep disorders that occur within 3 to 5 days after general anesthesia. The secondary endpoint is the incidence of circadian rhythm sleep disorders (rate of occurrence of sleep-retardation syndrome with drowsiness and strong fatigue). DISCUSSION: Postoperative sleep disorders after general anesthesia has been reported in patients with ASD; however, effective preventive pharmacological treatments have not been established. A sleep cycle regulator, ramelteon (Rozerem), is used as a therapeutic drug for patients with sleep disorders by decreasing the difficulty of falling asleep in insomnia. If sleep disorder can be prevented after the administration of general anesthesia in patients with ASD, we can support social participation while maintaining their quality of life. TRIAL REGISTRATION: The study was registered with the jRCT1071200030.