A study on the registration of cases of upper limb spasms after stroke treated with needle knife overall release surgery

Status

Recruiting

Phases

Phase 1

Study type

Observational

Source

ChiCTR

Registry ID

ChiCTR2300073884

Enrollment

Unknown

Registered

2023-07-24

Start date

2023-08-01

Completion date

Unknown

Last updated

2023-07-30

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

Conditions

Upper limb spasms after stroke

Interventions

Needle knife treatment group:NA

Da Jie Jing Acupuncture treatment group:NA

Xingnao Kaiqiao Acupuncture treatment group:NA

Ordinary acupuncture treatment group:NA

Eligibility

Sex/Gender

All

Age

35 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Meet the diagnostic criteria for stroke in traditional Chinese medicine and stroke in Western medicine (cerebral infarction and cerebral hemorrhage); 2. Having symptoms of upper limb hemiplegia and increased muscle tone, the evaluation criteria are based on Brunnstrom staging in stages I-III, and the modified Ashworth scale belongs to levels I-IV; 3. At least 2 weeks of onset, aged 35-75 years old; 4. Patients with clear awareness, stable vital signs, stable condition, and ability to cooperate with treatment and efficacy observation; 5. Both the patient and their family members agree to participate in this case registration study and sign an informed consent form.

Exclusion criteria

Exclusion criteria: 1. Individuals with abnormal coagulation mechanisms; 2. Signs of infection such as redness, swelling, burning, or deep abscess at the site of the surgery; 3. Patients with heart, brain, kidney and other organ failure; 4. Patients with bone and joint diseases such as bone tumors, spinal tuberculosis, and severe osteoporosis; 5. Patients with severe internal medicine diseases such as gastrointestinal bleeding and cirrhosis; 6. Patients with pulmonary tuberculosis, chronic hepatitis B and other infectious diseases. 7. Merge with other chronic infection patients, merge with mental illness patients, etc; 8. Women who are not suitable for relevant treatment during pregnancy or lactation; 9. Other situations where the researcher deems it inappropriate to participate in the study.

Design outcomes

Primary

Measure	Time frame
Modified Ashworth Spasticity Scale,MAS;Fugl-Meyer Assessment Scale, FMAS;modified Penn spasm frequency scale,MPSFS;	—

Secondary

Measure	Time frame
Range of motion,ROM;Visual Analogue Scale,VAS;Functional Independence Measure,FIM;Modified Barthel Index,MBI;	—

Countries

China

Contacts

Public ContactLIU Jia

Institute of Basic Research in Clinical Medicine, China Academy of Chinese Medical Sciences

marie_liujia@sina.cn+86 188 1087 7011

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026