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An Exploratory Study on the Effect of High-Frequency Repetitive Transcranial Magnetic Stimulation Synthesized with Electroacupuncture on Upper Limb Sensory Impairment Following Stroke

An Exploratory Study on the Effect of High-Frequency Repetitive Transcranial Magnetic Stimulation Synthesized with Electroacupuncture on Upper Limb Sensory Impairment Following Stroke

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400092635
Enrollment
Unknown
Registered
2024-11-20
Start date
2023-12-25
Completion date
Unknown
Last updated
2024-12-02

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

Conditions

stroke

Interventions

Experimental group:Repetitive transcranial magnetic stimulation with asynchronous Electroacupuncture
Synchronization group:Repetitive transcranial magnetic stimulation combined with Electroacupuncture

Sponsors

Hanzhong Central Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. all selected cases met the diagnostic criteria for stroke in the 2019 edition of diagnostic essentials of various cerebrovascular diseases in China , and were confirmed by brain CT or brain MRI examination; 2. Unilateral first-episode stroke with unilateral hemiplegia and sensory disturbance; 3. Age 18-85 years old, gender unlimited; 4. The course of disease is 2 weeks to 3 months; 5. No strict center of gravity, liver, kidney and other important organ dysfunction; 6. Speech and cognitive functions are basically normal, and can cooperate with various examinations and rehabilitation training; 7. The patients and their families are aware of this study and are willing to sign the informed consent and rTMS treatment informed consent.

Exclusion criteria

Exclusion criteria: 1. patients with upper limb motor sensory dysfunction caused by non stroke neurological diseases such as peripheral neuropathy and peripheral nerve injury; 2. Have severe cardiovascular and / or respiratory diseases; 3. There are cognitive and speech disorders that cannot cooperate with the examination and treatment; 4. There are contraindications to rTMS, such as wearing pacemaker, intracranial metal, etc; 5. Fever, infection or important organ failure, critical illness; 6. Unable to cooperate with assessment or treatment for various reasons.

Design outcomes

Primary

MeasureTime frame
Sensory disturbance rating scale;Somatosensory evoked potential N20;

Secondary

MeasureTime frame
Upper limb movement research scale;Modified Barthel Index;

Countries

China

Contacts

Public ContactWang Yang

Hanzhong Central Hospital

516599293@qq.com+86 157 0926 0670

Outcome results

None listed

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