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 @ 6:38 PM
Ignite Modification Date:
2025-12-24 @ 6:38 PM
NCT ID:
NCT07113457
Eligibility Criteria:
Inclusion Criteria:
* A first time, unilateral, ischemic, hemispheric stroke, confirmed by MRI
* Chedoke stage of hand assessment \>= 3
* Ability to open and close affected hand
* Able to understand and communicate in english
* Able to independently consent
* over 6 months post stroke
* Must have a hemoglobin level above 10g/dl
* Must have ability to leave research visit with a compainon/group trasportation
* WOCBP must be comfortable confirming negative pregnancy prior to hypoxia
* Must not be involved in any other research intervention study testing upper extremities
Exclusion Criteria:
* History of prior neurological disorders
* Brain stem or cerebellar stroke; mean Fazekas score rated on initial fluid-attenuated inversion recovery MRI greater than equal to 3
* Severe Aphasisa
* Pre-existing hypoxic pulmonary disease
* Includes positive Covid-pneumonia diagnosis within 1 year of screening visit
* Severe hypertension (\>160/100)
* Any ischemic cardiac disease
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT07113457
Study Brief:
Protocol Section:
NCT07113457