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:
2025-12-25 @ 2:17 AM
Ignite Modification Date:
2025-12-25 @ 2:17 AM
NCT ID:
NCT02028260
Eligibility Criteria:
Inclusion Criteria
* Adult patients ≥ 18 yrs of age, \< 76 yrs of age
* Admitted to MICU (3B and 3C) or SICU (8C, 8D, 11C)
* Surrogate present to provide informed consent when patient is not able
* RASS score of \>-3, \< +1
* CAM positive
* Enteral access
Exclusion Criteria:
* Recent MI (within past 2 weeks)
* High risk of dysrhythmias (i.e. bundle branch block, QT prolongation, class IV HF, implanted device)
* Unable to tolerate enteric medication
* History of stimulant induced mania/psychosis
* Pre-existing neurologic disease
* Patients transferred from outside hospital
* Pregnancy
* Alcohol withdrawal
* History of end stage liver disease (Childs-Pugh class B or worse)
* Prognosis considered hopeless (CMO)
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Maximum Age:
75 Years
Study:
NCT02028260
Study Brief:
Protocol Section:
NCT02028260