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Clinical Trials/DRKS00030023
DRKS00030023
Recruiting
Not Applicable

Rehabilitation and Clinical Observation of stroke patients to validate prognostic factors of functional and subjective Recovery after Stroke (RECOVER-S): A registry-based cohort study - RECOVER-S

Charité Campus Charité Mitte0 sites1,000 target enrollmentAugust 25, 2022

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
I63
Sponsor
Charité Campus Charité Mitte
Enrollment
1000
Status
Recruiting
Last Updated
last year

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
August 25, 2022
End Date
TBD
Last Updated
last year
Study Type
Observational
Sex
All

Investigators

Sponsor
Charité Campus Charité Mitte

Eligibility Criteria

Inclusion Criteria

  • 1\. male or female adult:r \= 18 years at the time of study inclusion.
  • 2\. acute stroke (ischemic or intracerebral hemorrhagic) confirmed by computed tomography (CT) or magnetic resonance imaging (MRI) image morphology
  • 3\. inclusion in the study within \= 9 days after stroke (inclusion in an acute care hospital) or within \= 35 days after stroke (inclusion in a rehabilitation hospital/geriatric ward)
  • 4\. neurological or geriatric rehabilitation (outpatient or inpatient) planned or recommended.

Exclusion Criteria

  • 1\. no neurological or geriatric rehabilitation (outpatient or inpatient) planned.
  • 2\. intracranial hemorrhage primary in the context of a subarachnoid hemorrhage, subdural or epidural hematoma (small, concomitant portions in primary ICB are not an exclusion criterion)
  • 3\. post\-stroke according to diagnosis list (clinically silent strokes not known or diagnosed prior to stay are not exclusion criteria)
  • 4\. invasive long\-term ventilation at the time of study inclusion
  • 5\.Life expectancy before stroke \<12 months.
  • Biomarker cohort\-specific exclusion criteria:
  • 1\. patient:ing with a primary hemorrhagic stroke.
  • 2\. presence of MRI contraindications (e.g., pacemaker, claustrophobia, metallic implants, etc.)
  • 3\. inability (for MRI measurement) to lie still for \> 30 minutes.

Outcomes

Primary Outcomes

Not specified

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