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 @ 5:44 PM
Ignite Modification Date:
2025-12-24 @ 5:44 PM
NCT ID:
NCT05335668
Eligibility Criteria:
Inclusion Criteria patients:
* Patients with a haemorrhagic or ischemic stroke affecting the somatosensory system as defined by both CT or MRI and clinical criteria
* Patient age between 18-75 years
* Signed written informed consent
Exclusion Criteria patients:
* Secondary stroke due to a cerebral vascular malformation or tumor
* Patients with aphasic syndromes and impaired verbal communication, complete sensory-motor hemi-neglect and restrictions of the ability to report on their pain and cooperate during sensory testing
* Patients with severe stroke NIHSS \> 14 and or Modified Rankin Scale (MRS) \> 3
* History of severe myelopathy or polyneuropathy with clinical sensory deficits and history of neuropathic pain
* Widespread stroke size due to internal carotid artery-occlusion or more than one main territory (anterior, middle or posterior cerebral artery)
* Contraindication for 7T MRI (metallic implant, tattoo, claustrophobia, etc.)
* In case of women \< 45 years of age: pregnancy
Inclusion Criteria for healthy volunteers
* Informed consent as documented by signature
* Age: ≥18 years and ≤ 75 years
Exclusion criteria for healthy volunteers
* Pregnancy and breastfeeding
* Contraindication for 7T MRI (metallic implant, tattoo, claustrophobia, etc.)
Healthy Volunteers:
True
Sex:
ALL
Minimum Age:
18 Years
Maximum Age:
75 Years
Study:
NCT05335668
Study Brief:
Protocol Section:
NCT05335668