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Observational Study on Determinants of Dementia After Stroke

Conditions Phase Intervention Type
  • Stroke
  • Ischemic Stroke
  • Middle Cerebral Artery Syndrome
N/A

View trial NCT01334749 on www.clinicaltrials.gov

229 PatientsLikeMe members may be eligible for this trial.

  • Show contact details

Contacts

Please use the information below to contact the trial coordinators.

    Martin Dichgans, Prof.
    +49-89-7095x8310
    martin.dichgans@med.uni-muenchen.de Christian Opherk, MD
    +49-89-7095x8315
    christian.opherk@med.uni-muenchen.de
×

Eligibility

Ages Eligible for Study
18 years and up
Genders Eligible for Study
Both

Keywords

Stroke, Dementia, Dementia, Vascular, Alzheimers Disease, Intracranial Hemorrhage, and Brain Ischemia

Sponsors

Other
Ludwig-Maximilians - University of Munich

Inclusion Criteria

- Age ≥ 18 years

- Language: German

- Acute stroke that occurred within the last 3 days as defined by:

acute focal neurological deficit in combination with one of the following:

- An acute ischemic infarct as documented by either a DWI positive lesion on MR imaging
or a new lesion on a delayed CT scan

- An intracerebral hemorrhage as documented on CT or MRI

- An informant of the patient is available

- Written informed consent by patient prior to study participation

- Willingness to participate in follow-up

Exclusion Criteria

- IQCODE > 64 or diagnosis of dementia

- Patients living at distance > 30km of the participating center

- Patients transferred from an outside hospital (to avoid possible selection bias)

- Patients presenting a stroke going back more than 72 hours

- Patients presenting one of the following diseases: cerebral venous thrombosis,
traumatic cerebral haemorrhage, intracerebral haemorrhage because of a known or
image-guided assumed vascular malformation, pure meningeal or intraventricular
haemorrhage

- Patients presenting a malignant disease with life expectancy < 3years
Contraindication for MRI

- Participation in an intervention/AMG-study

Detailed Description

The primary aim of the DEDEMAS (Determinants of Dementia After Stroke) study is to identify predictors of post stroke dementia (PSD). A particular focus will be on biological markers (neuroimaging, biochemical markers derived from blood) and on interactions between vascular and neurodegenerative mechanisms. For this purpose patients with an acute stroke and without prior dementia will be followed for 60 months.

Contacts and Locations

Please refer to this study by its ClinicalTrials.gov identifier: NCT01334749

Overall Contact

Christian Opherk, MD
+49-89-7095x8315
christian.opherk@med.uni-muenchen.de

Overall Contact Backup

Martin Dichgans, Prof.
+49-89-7095x8310
martin.dichgans@med.uni-muenchen.de

Locations

  • Interdisciplinary Stroke Center Munich, Klinikum der Universität München, Campus Großhadern
    Munich, Bavaria Germany
    (Recruiting)

    Contact info

    Martin Dichgans, Prof.
    +49-89-7095x8310
    martin.dichgans@med.uni-muenchen.de

Learn more at ClinicalTrials.gov

◄ Back to list of trials

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