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:
2025-12-24 @ 7:16 PM
Ignite Modification Date:
2025-12-24 @ 7:16 PM
NCT ID:
NCT03684603
Eligibility Criteria:
Inclusion Criteria:
* Male and Female patients above 18 years of age
* signed informed consent after being informed
* subacute (i.e. symptom onset 3 - 90 days ago) lateralized ischemia or hemorrhage as confirmed by brain imaging (CT or MRI).
* Fugl-Meyer Upper Extremity Score between 15 and 59
Exclusion Criteria:
* other neurological or systemic disorder which is likely to cause dementia, cognitive dysfunction or central motor symptoms
* severe sensory aphasia
* preexisting arm paresis
* intake of sedatives, or neuroleptics
* Relevant hearing loss
* Vulnerable Person
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT03684603
Study Brief:
Protocol Section:
NCT03684603