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Multicenter clinical evaluation of Fengshi fascial point acupuncture in relieving hand spasm after stroke

Multicenter clinical evaluation of Fengshi fascial point acupuncture in relieving hand spasm after stroke

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900022379
Enrollment
Unknown
Registered
2019-04-09
Start date
2019-05-07
Completion date
Unknown
Last updated
2019-04-15

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

Conditions

stroke

Interventions

Acupuncture group:Feng's fascial point acupuncture combined with routine rehabilitation therapy
Sham acupuncture group:Feng's fascial point sham needling combined with routine rehabilitation therapy

Sponsors

Shanghai Seventh People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Cerebral hemorrhage or cerebral infarction was confirmed by CT or MRI examination, and the diagnosis met the diagnostic criteria revised by the 4th National Academic Conference on Cerebrovascular Disease; 2. the first onset was unilateral hemiplegia; the onset time longer than 2 weeks, with stable vital signs; 3. Aged 30-80 years old; 4. spastic paralysis of upper limbs, Brunnstrom stage II-IV of upper limbs, and improved Ashworth evaluation of hemiplegic side. Grade 1 + - 3; 5. stable condition, clear consciousness, no aphasia, mental retardation, be able to understand the content of the scale and cooperate with examination and treatment; 6. informed consent and written informed consent.

Exclusion criteria

Exclusion criteria: 1. The condition in critical or acute stage is not stable; 2. those with deafness, aphasia or severe cognitive impairment are difficult to communicate normally; 3. those with serious primary diseases of cardiovascular, liver, kidney, blood, digestive and respiratory systems are psychiatric patients, malignant tumors, patients with venous thrombosis, osteoporosis, severe bleeding tendency and infection of treatment site; 4. Systolic blood pressure > 180 mmHg or diastolic blood pressure > 110 mmHg; unable to cooperate with the program for rehabilitation or to participate in other clinical trials or studies within three months to receive other related treatment, which may affect the efficacy of this study; 5. dystonia caused by other reasons and previous motor dysfunction; pregnant and lactating women; 6. fear of acupuncture, halo needle, etc.; 7. took sedative and muscle relaxant in past 2 weeks.

Design outcomes

Primary

MeasureTime frame
Degree of hand spasm;

Countries

China

Contacts

Public ContactFeng Wei

Shanghai Seventh People's Hospital

fwginger@126.com+86 15102131500

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 28, 2026