Stroke Ischemic
Conditions
Keywords
rTMS, stroke Ischemic
Brief summary
The goal of this clinical trial is to learn if transcranial magnetic stimulation(rTMS) can improve neurological rehabilitation in patients with acute ischemic stroke. The main questions it aims to answer are: Can rTMS Promote Recovery of Limb Impairment in Patients with Acute Ischemia? Can rTMS Cause Changes in the Functional Connections of Brain Networks in Patients? Researchers will compare rTMS therapy to non-stimulation therapy to see if rTMS is effective in promoting neurological recovery from ischemic stroke. Participants will: Receive rTMS or sham stimulation with LF-rTMS on the contralateral M1 of the brain lesion for 20 minutes, 1200 pulses, 120% RMT, and a treatment period of 5 days； Be evaluated on a scale before and after treatment
Interventions
DEVICErTMS
LF-rTMS of M1 contralateral to the brain lesion for 20 min, 1200 pulses, 120% RMT, treatment cycle of 5 days
Sponsors
The First Affiliated Hospital with Nanjing Medical University
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)
Eligibility
Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No
Inclusion criteria
1. The age range is 18\ 75 years old 2. Meet the diagnostic criteria of China Acute Ischaemic Stroke Diagnosis and Treatment Guidelines 2018 and confirmed by head CT or MRI scanning 3. Acute stage of the disease <14 days and stable condition 4. Stroke patients with only unilateral limb involvement (without bilateral cerebrovascular lesions) 5. Patients with upper limb muscle strength ≥ grade 3, able to perform fNIRS tasks with the patient. 6. Subjects were right-handed 7. Participants give their informed consent and sign an informed consent form
Exclusion criteria
1. Those who have metal implants or any electronic devices in their body 2. Those with previous epilepsy or mental abnormality. 3. Combined with serious heart, liver, lung and other important organ failure 4. Those who have brain haemorrhage or bleeding tendency. 5. Deteriorating condition, new cerebral infarction or secondary cerebral haemorrhage. 6. Patients with history of craniocerebral trauma and craniocerebral surgery. 7. Those with severe cognitive and communication disorders who are unable to cooperate -
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Improvement in patient motor function | Before patient treatment and 5 days after patient treatment | Fugl-Meyer assessment scale，FMA Score: Minimum: 0 points, Maximum: 100 points The higher the score, the better the limb function. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Altered functional connectivity of brain networks in patients | Patient before and after treatment on the first and fifth day of treatment and during rTMS treatment | data from near-infrared functional brain imaging acquisitions |
Countries
China
Contacts
Primary ContactZhaolu Wang
Outcome results
None listed