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A clinical study to assess the influence of acupuncturing “Wang’s Jiaji” acupoints on limb spasticity of patients in convalescent stage of ischemic stroke

A clinical study to assess the influence of acupuncturing “Wang’s Jiaji” acupoints on limb spasticity of patients in convalescent stage of ischemic stroke

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN31511176
Enrollment
100
Registered
2017-09-21
Start date
2017-11-01
Completion date
Unknown
Last updated
2019-08-26

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

Conditions

Ischemic stroke Circulatory System

Interventions

A total of 100 participants will be randomly assigned to two different groups. All of the patients will be given basic treatment according to the guideline for prevention and treatment of cerebrovascu

Sponsors

Beijing Municipal Health and Family Planning Commission
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Meet the western medicine diagnostic criterion: American Heart Association/American Stroke Association, AHA/ASA in 2013 2. Patients with cerebral infarction and the session is between 1 month and 6 months 3. Patients between 40 and 75 years old. Patients over 75 can also be accepted in the trial if the doctor approves the significance of rehabilitation therapy after assessment, but all the patients should not be over 80 years old 4. 4 points = NIHSS =21 points 5. 2 grade = MAS =4 grade 6. GCS =7 points without any consciousness trouble 7. First attack of stroke or not for the first time without any serious disabilities, mRS =3 points 8. Confirmed by head CT or MRI 9. Patients who agreed to participant in this trial and assigned the informed consent

Exclusion criteria

Exclusion criteria: 1. Patients with limb dystonia caused by cerebral or other diseases 2. Patients participated in other trials within 3 months 3. Patients with serious heart,liver,kidney and hematopoietic system diseases or mental disorders 4. Taking drugs for improving muscular tension apart from baclofen 5. Afraid of acupuncture or allergic to baclofen 6. Women in pregnant or lactating period 7. Patients with congenital disability

Design outcomes

Primary

MeasureTime frame
Upper and lower limb motor function of affected side, assessed using Simplified Fugl-Meyer (FMA) at baseline, 2 weeks, 4 weeks and 12 weeks after first acupuncture

Secondary

MeasureTime frame
1. Muscular tension assessed using Modified Ashworth scale at baseline, 2 weeks, 4 weeks and 12 weeks after first acupuncture 2. The ability of daily living assessed using Modified Barthel scale at baseline,2 weeks,4 weeks and 12 weeks after first acupuncture 3. The level of spasticity assessed using electromyography at baseline and 12 weeks after first acupuncture

Countries

China

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Mar 2, 2026