Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 1:40 PM
Ignite Modification Date:
2025-12-24 @ 1:40 PM
NCT ID:
NCT03165695
Eligibility Criteria:
Inclusion Criteria:
* 65 years of age or older.
* Admitted to BWH vascular surgical service.
* Able to provide informed consent or a surrogate is available to provide informed consent.
* Absence of delirium at time of consent.
Exclusion Criteria:
* Expected stay or life expectancy less than 48 hours
* Unable to take medications orally
* Advanced liver disease (Child-Pugh class B or worse)
* Active treatment with Fluvoxamine
* Active treatment with antipsychotic medications, benzodiazepines or other hypnotic agents (i.e. Trazodone, Mirtazapine, Zolpidem, Zaleplon)
* Known or suspected diagnosis of Lewy body dementia
* Any dermatological condition that may be aggravated by using a wrist sensor.
* Known pre-existing sleep disorder other than insomnia.
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
65 Years
Study:
NCT03165695
Study Brief:
Protocol Section:
NCT03165695