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 @ 2:44 PM
Ignite Modification Date:
2025-12-24 @ 2:44 PM
NCT ID:
NCT03546959
Eligibility Criteria:
Inclusion Criteria:
1. Adult stroke (18-80 years)
2. Patients with stroke who can sit without support
3. Patients with stroke who have spasticity which limit upper limb function
Exclusion Criteria:
1. Brunnstrom motor recovery stage 1 and 6
2. Comorbidities such as hemiplegic shoulder pain, complex regional pain syndrome, central post-stroke pain, brachial plexus injury etc.
3. Upper limb spasticity with MAS level 4 or presence of contracture in upper extremity.
4. Contraindications for lycra sleeve ( circulatory disorder etc.)
5. Contraindications for botulinum toxin (infection at the injection site, hypersensitivity to toxin etc.)
6. Severe aphasia or cognitive dysfunction that limit participation in rehabilitation (7) Receiving botulinum toxin injection within the last 6 months
Healthy Volunteers:
False
Sex:
FEMALE
Minimum Age:
18 Years
Maximum Age:
80 Years
Study:
NCT03546959
Study Brief:
Protocol Section:
NCT03546959