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NCT07435467Recruiting

Blood Biomarkers for Alzheimer Disease and Neuro-injury to Estimate the Association With Cognitive/Functional Decline and Mortality in a Real-world Population of GERiatric Hospitalized Patients (BAD-GER)

Blood Biomarkers for Alzheimer Disease and Neuro-injury to Estimate the Association With Cognitive/Functional Decline and Mortality in a Real-world Population of GERiatric Hospitalized Patients (BAD-GER): a Multicenter, Observational, 3-arms, Prospective Study

Source: ClinicalTrials.gov · Last updated 27 Feb 2026

Brief summary (registry, in English)

The BAD-GER study is a multicenter, prospective, three-arm observational study serving to validate a prognostic biomarker algorithm for mortality and hospital readmission; this algorithm will be developed through the retrospective analysis of Alzheimer's Disease and neurodegeneration biomarkers in an already available discovery cohort of 700 previously hospitalized geriatric patients.

Status (registry)
Recruiting
Study type
Observational
Enrollment
400 (estimated)
First submitted
19 Feb 2026
Start date
9 Apr 2025
Primary completion date
30 Jun 2026
Lead sponsor
Istituto Nazionale di Ricovero e Cura per Anziani
NCT number
NCT07435467

What you commit to

  • Study type: Observational
  • Planned participants: 400
  • From 9 Apr 2025 to the primary completion date, 30 Jun 2026
  • 3 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • no informed consent
    • GROUP 2: Patients hospitalized for non-neurological diseases with dementia
  • Inpatients with one of the following diagnoses: ischemic or hemorrhagic stroke, delirium, status epilepticus, encephalitis/meningitis
  • no informed consent
    • GROUP 3: Patients hospitalized for non-neurological diseases without dementia
  • inpatients with one of the following diagnoses: ischemic or hemorrhagic stroke, delirium, status epilepticus, encephalitis/meningitis
  • diagnosis of dementia

Other

  • no informed consent

Who the study is looking for

  • Inpatients with one of the following diagnoses: ischemic or hemorrhagic stroke, delirium, status epilepticus, encephalitis/meningitis
  • inpatients with diagnosis of major neurocognitive disorder according to DSM-5 criteria (2013)
  • inpatients with non-neurological diseases

Criteria the registry did not label

  • GROUP 1: Patients hospitalized for acute neurological disorders

Age in the registry: 65 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (3)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
IRCCS INRCA Hospital
Coordinator of this site? Confirm its status
AnconaItalyRecruiting
IRCCS INRCA Hospital
Coordinator of this site? Confirm its status
FermoItalyRecruiting
Policlinico Universitario
Coordinator of this site? Confirm its status
MessinaItalyRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.