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Clinical Trial Protocol: Alzheimer's Dementia Underlying Encephalopathy

Clinical Trial Protocol: Alzheimer's Dementia Underlying Encephalopathy

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07222280
Enrollment
30
Registered
2025-10-29
Start date
2025-06-10
Completion date
2026-03-31
Last updated
2025-10-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Alzheimer Dementia, Alzheimer Disease, Cognitive Abnormality, Delirium Confusional State, Encephalopathy

Brief summary

The goal of this clinical trial is to determine if utilizing the Quest AD-Detect blood test, while patient's are hospitalized for a cognitive diagnosis (such as delirium or encephalopathy), will result in an earlier diagnosis of underlying Alzheimer's disease. * Will this blood test have the ability to distinguish between Alzheimer's disease and other causes of cognitive impairment in the inpatient setting? * Neurology Clinic will complete a 6-month post-hospitalization follow up with patients who have had the Quest AD-Detect Alzheimer's Disease blood test completed while they were inpatient to discuss the risk assessment portfolio

Interventions

DIAGNOSTIC_TESTQuest AD-Detect blood test

Blood will be collected and sent for testing using the Quest AD-Detect blood test

Sponsors

Covenant Health, US
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
60 Years to 90 Years
Healthy volunteers
No

Inclusion criteria

* Ages 60 to 90 years old * No prior diagnosis of dementia * Currently hospitalized with cognitive diagnosis, including but no limited to; delirium, encephalopathy, etc. thought to be secondary to a toxic/metabolic state

Exclusion criteria

* Age under 60 years * Prior diagnosis of dementing illness or other organic etiology to cognitive impairment

Design outcomes

Primary

MeasureTime frameDescription
To show the percentage of patients (21 patients in the study) who presented with a cognitive diagnosis (including but not limited to delirium, encephalopathy, etc.) that have a positive biomarker for Alzheimer's dementiaFrom enrollment to 6 month follow up appointment with Neurology Clinic.A Six month follow up with the Neurology clinic to discuss the results of Quest AD Detect (p-tau217), those patients who are found to have a positive outcome will receive additional follow-up in the Neurology clinic (which could include the use of additional lab tests or further diagnostic testing).

Countries

United States

Contacts

Primary ContactClinical Research Nurse Coordinator
aholt10@covhlth.com865-331-1337

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026