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Clinical study on the effect of neural regulation technology on autonomic nerve function in patients with stroke

Clinical study on the effect of neural regulation technology on autonomic nerve function in patients with stroke

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2100050030
Enrollment
Unknown
Registered
2021-08-16
Start date
2021-09-01
Completion date
Unknown
Last updated
2022-04-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Stroke

Interventions

tDCS Group: transcranial direct current stimulation
Median nerve stimulation group:median nerve electrical stimulation
control group:None

Sponsors

Department of Rehabilitation Medicine, Huashan Hospital, Fudan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
15 Years to 80 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria for stroke patients: 1. Patient aged 18-75 years old; 2. After cerebral infarction or cerebral hemorrhage, 1 month<=onset time<=6 months; 3. The diagnosis conforms to the diagnostic points of various cerebrovascular diseases adopted by the Fourth National Cerebrovascular Disease Academic Conference in 1995; 4. Patients who have suffered a stroke for the first time or have had no sequelae in the past; 5. Stroke confirmed by head CT or MRI examination and excluded other obvious neurological diseases (such as encephalitis, hydrocephalus, etc.); 6. Have limb dysfunction; 7. Sinus rhythm; 8. The patient himself or his legal representative signed the informed consent. Inclusion criteria for healthy subjects: 1. Aged 18 to 75 male or female; 2. In good health, the chief complaint is no special discomfort, no special past history, and no abnormal laboratory imaging examination results; 3. No drinking, smoking, etc.; 4. Voluntary participation, the patient himself understands and signs the informed consent, and can complete the experiment according to the experimental protocol.

Exclusion criteria

Exclusion criteria: 1. Patients with various severe arrhythmias; 2. Patients with serious primary diseases such as heart, liver, kidney and hematopoietic system; 3. Patients with autonomic dysfunction caused by other non-cerebrovascular causes (such as peripheral neuropathy, diabetic autonomic neuropathy, etc.); 4. Those who have a history of mental disorders and drug abusers in the past; 5. Stroke patients with major organ failure or critical illness; 6. Patients with malignant tumor.

Design outcomes

Primary

MeasureTime frame
Epinephrine, norepinephrine, cortisol, aldosterone, renin, corticotropin, angiotensin II, IgF-1 levels;Heart rate variability (HRV) assessment;Upper Limb Movement Research Scale (ARAT);

Countries

China

Contacts

Public ContactWu Yi

Department of Rehabilitation Medicine, Huashan Hospital, Fudan University

wuyi3000@163.com+86 13003176229

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026