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Clinical study on the treatment of post-stroke hemilateral numbness with electroacupuncture Fang's scalp sensory zone

Clinical study on the treatment of post-stroke hemilateral numbness with electroacupuncture Fang's scalp sensory zone

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2026000629
Enrollment
Unknown
Registered
2026-03-19
Start date
2026-05-05
Completion date
Unknown
Last updated
2026-03-30

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

Conditions

post-stroke hemilateral numbness

Interventions

control group: conventional acupuncture
treatment group:electroacupuncture Fang's scalp sensory zone+ conventional acupuncture

Sponsors

Xi'an Hospital of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
30 Years to 80 Years

Inclusion criteria

Inclusion criteria: Participants will be eligible if they meet all of the following criteria: (1) Meet the diagnostic criteria of traditional Chinese medicine and western medicine for stroke, as well as the staging criteria for stroke; (2) The first occurrence of numbness in one side of the body after a stroke, manifested as numbness in a single upper or lower limb or numbness in both limbs simultaneously, with or without movement disorders in one side of the body; (3) 30 =Age=80 years,gender not limited; (4) Patients who voluntarily participate in this trial and give informed consent.

Exclusion criteria

Exclusion criteria: Participants will be excluded if they meet any of the following criteria: (1) Patients who have limb numbness symptoms before the onset of the stoke; (2) Limb numbness caused by other diseases, such as sensory disorders resulting from diabetic peripheral neuropathy, trauma and other accidental conditions; (3) Patients with severe consciousness disorders,psychiatric disorders or cognitive dysfunction; (4) Patients who are pregnant , breastfeeding or planning to become pregnant; (5) Patients who are prone to fainting from needles or unable to persist in this study; (6) Patients who are participating in other studies and have been enrolled in other clinical studies patients within the past 3 months.

Design outcomes

Primary

MeasureTime frame
the modified Fugl-Meyer and Lindmark methods;

Secondary

MeasureTime frame
Visual Analogue Scale score;the Modified Barthel Index Scale score;Self-Rating Anxiety Scale score;Self-Rating Depression Scale score;

Countries

China

Contacts

Public ContactTong Yanjie

Xi'an Hospital of Traditional Chinese Medicine

1197683743@qq.com+86 152 0927 9618

Outcome results

None listed

Source: ITMCTR (via WHO ICTRP) · Data processed: Apr 4, 2026