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The Evidence-Based Study of the Xingnao Kaiqiao Rehabilitation Program in Treating Post-Stroke Motor Dysfunction.

The Evidence-Based Study of the 'Xingnao Kaiqiao' Rehabilitation Program in Treating Post-Stroke Motor Dysfunction.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2026001582
Enrollment
Unknown
Registered
2026-06-23
Start date
2026-07-06
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Post-ischemic stroke motor dysfunction

Interventions

Acupuncture group: The point selection is according to "Xingnao Kaiqiao" acupuncture theory:Neiguan (bilateral), Shuigou, Sanyinjiao (affected side), Fengchi, Wangu, Tianzhu, Xiajiquan, Chize, Hegu, a
Sham acupuncture group:Non-meridian non-acupoints (control points) are selected for shallow insertion of 0.2-0.3 cun (4-6 mm). The needle is hanging at the skin without sensation of "De Qi", and no ac

Sponsors

First Teaching Hospital of Tianjin University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
45 Years to 75 Years

Inclusion criteria

Inclusion criteria: (1) Meets the diagnostic criteria for ischemic stroke: diagnosis refers to the "2019 AHA/ASA Guidelines for Early Management of Acute Ischemic Stroke" designated by the American Heart Association/American Stroke Association (AHA/ASA); (2) Age 45-75 years, gender (referencing previously published JAMA Network Open); (3) Within 0-14 days of ischemic stroke onset; (4) Presence of motor dysfunction, modified Rankin scale (mRS) score of 2-4; (5) Understands and follows clinical trial procedures, voluntarily participates and signs the informed consent form (can be signed voluntarily by the individual or their guardian).

Exclusion criteria

Exclusion criteria: (1) Subjects with intracranial hemorrhage shown on CT/MRI imaging or those presenting with signs of subarachnoid hemorrhage; (2) Subjects with a history of stroke, or those with other causes of motor dysfunction, or those with a pre-stroke mRS score > 2; (3) Subjects with cerebral infarction accompanied by severe cerebral edema, mass effect, and signs of brain herniation; (4) Subjects with NIHSS consciousness level score (1a) > 2, or those with epilepsy, dementia, schizophrenia, or other conditions severely impairing cognitive function and mental awareness, making them unable to cooperate with treatment or evaluation of efficacy; (5) Subjects with bleeding or oozing after thrombolysis or thrombectomy; (6) Subjects with severe liver dysfunction, including liver failure, cirrhosis, portal hypertension (esophageal varices), and active hepatitis; subjects with heart failure, bacterial endocarditis, pericarditis, or acute pancreatitis; subjects with renal dysfunction (nephritis, nephropathy, and renal failure, etc.); subjects with intracranial tumors, arteriovenous malformations, aneurysms, or other major diseases; (7) Subjects with a life expectancy of less than one year due to malignant diseases or other severe illnesses; (8) Subjects with local infection at acupuncture points; (9) Pregnant or breastfeeding women, or those with plans to conceive who are unwilling to take effective contraceptive measures; (10) Subjects currently participating in or who participated in other clinical studies within the past three months.

Design outcomes

Primary

MeasureTime frame
Modified Rankin Scale;

Secondary

MeasureTime frame
National Institutes of Health Stroke Scale;Barthel Index;Fugl-Meyer Assessment Scale;Carroll upper extremity function test;

Countries

China

Contacts

Public ContactShi Jiang Wei

First Teaching Hospital of Tianjin University of Traditional Chinese Medicine

acustone@163.com13920867865

Outcome results

None listed

Source: ITMCTR (via WHO ICTRP) · Data processed: Aug 10, 2026