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A Clinical Randomized Controlled Trial of Guan Needling Combined with Physical Therapy for the Treatment of Lower Limb Spasticity in Stroke Patients.

A Clinical Randomized Controlled Trial of Guan Needling Combined with Physical Therapy for the Treatment of Lower Limb Spasticity in Stroke Patients.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2026000571
Enrollment
Unknown
Registered
2026-03-18
Start date
2026-04-01
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

Stroke

Interventions

Observation group:Combination of Guan Ci and Physical Therapy

Sponsors

Shuguang Anhui Hospital Affiliated to Shanghai University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
No minimum to 80 Years

Inclusion criteria

Inclusion criteria: (1) Patients who meet the diagnostic criteria for stroke in both traditional Chinese and Western medicine and have been confirmed by CT or MRI; (2) Patients with a disease course of within 360 days; (3) Patients with lower limb spasticity manifested by increased muscle tone, increased resistance during passive movement, and a lower limb score of =1 on the Modified Ashworth Scale (MAS); (4) Patients under the age of 80; (5) Patients who voluntarily participate in this study and sign the informed consent form.

Exclusion criteria

Exclusion criteria: (1) Lower limb spasticity not caused by stroke (e.g., spinal cord injury, Parkinson's disease, cerebral palsy, etc.); (2) Severe organic diseases of the heart, liver, or kidneys, or coagulation disorders; (3) Skin damage, infection, thrombosis, or local deformities at the lower limb treatment site that affect treatment; (4) Use of muscle relaxants (e.g., baclofen), botulinum toxin injections, or other anti-spasticity treatments within the past two weeks; (5) Needle phobia, fear of needles, or allergy to ultrasound coupling agents; (6) Poor compliance, unable to complete the 3-week treatment.

Design outcomes

Primary

MeasureTime frame
Modified Ashworth Scale;Musculoskeletal Ultrasound Assessment;

Secondary

MeasureTime frame
Fugl-Meyer Motor Function Assessment;Modified Barthel Index;Clinical Spasticity Index;

Countries

China

Contacts

Public ContactGuo Rui Luan

Shuguang Anhui Hospital Affiliated to Shanghai University of Traditional Chinese Medicine

luanguorui@163.com15856987363

Outcome results

None listed

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