Washington University Medical School
St Louis, Missouri, 63108, United States
NCT Number: NCT02063217
The purpose of this study is to change the concentration of amyloid-beta in human cerebrospinal fluid (CSF) through modulation of the sleep-wake cycle.
Looking for future studies?
Notify Me18 year–60 year
All sexes
Interventional
Not applicable
St Louis, Missouri, 63108, United States
The purpose of this research study is to investigate whether or not increasing or decreasing duration of sleep over one night will change the concentration of amyloid-beta in cerebral spinal fluid (CSF).
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Sodium oxybate h.s.
Other names: Xyrem
36hr sleep deprivation
Time frame: Baseline = 07:00 to 19:00; Intervention period = 01:00 to 11:00
Overnight (01:00 to 11:00) differences in CSF amyloid beta from baseline (07:00 to 19:00) between 1) sleep-deprived and control participants and 2) sleep-induced and control participants.
Washington University School of Medicine
Other
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.
Published trials that share one or more normalized conditions with this study.
NCT03077620
Amyloid-beta, Pathological Conditions, Anatomical
St Louis, Missouri, United States
View Trial DetailsNCT06649760
Caries,Dental, Dental Caries
Alexandria, Egypt
View Trial DetailsNCT07640399
Bleeding, Gingival Diseases
Mississauga, Ontario, Canada
View Trial DetailsNCT04032626
Alzheimer Disease, Amyloid Plaque
Phoenix, Arizona, United States
View Trial Details