Skip to content

Exploration of the therapeutic effect of lower limb meridian stimulation on the recovery of superficial sensory impairment after spinal cord injury

Exploration of the therapeutic effect of lower limb meridian stimulation on the recovery of superficial sensory impairment after spinal cord injury

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500095763
Enrollment
Unknown
Registered
2025-01-13
Start date
2024-06-30
Completion date
Unknown
Last updated
2025-01-27

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

Conditions

spinal cord injury

Interventions

Group A:conventional rehabilitation training
Group B:conventional rehabilitation training+meridian stimulation

Sponsors

Shanghai Hebin Rehabilitation Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 85 Years

Inclusion criteria

Inclusion criteria: 1. Patients with spinal cord injury accompanied by sensory impairment, in accordance with the "Expert Consensus on Diagnosis and Treatment of Traumatic Spinal Cord Injury (2022 Edition)" ; 2. First onset spinal cord injury patients with a course of disease within 1 to 12 months (excluding spinal shock phase); 3. Age between 18 and 85 years old; 4. Patients with incomplete injury; 5. The patient's lower limb epidermis is not damaged; 6. The patient's vital signs are stable and the condition is stable; 7. No obvious cognitive impairment, able to understand and cooperate with intervention and evaluation (MoCA score>26 points). 8. The subjects voluntarily joined this study and signed an informed consent form.

Exclusion criteria

Exclusion criteria: 1. There are damages or infections on the lower limb epidermis and scalp that affect intervention and evaluation; 2. Risk factors such as lower limb deep vein thrombosis/intermuscular vein thrombosis, unstable hypertension, and severe heart disease; 3. Obvious speech, attention, intellectual, mental, or cognitive impairments; 4. Having a history of organic brain diseases, neurological and psychiatric disorders, drug abuse, and alcoholism in the past; 5. Severe heart, lung, liver, kidney and other important organ dysfunction patients; 6.There are metal foreign objects such as pacemakers and metal stents in the body; 7. Patients with skull defects or skull repairs; 8. Patients who are unable to cooperate in completing treatment and evaluation, or have poor compliance; 9. Participated in other clinical trials during the same period; 10. Other situations deemed unsuitable for inclusion by researchers.

Design outcomes

Primary

MeasureTime frame
International Standards for Neurological Classification of Spinal Cord Injury;Somatosensory evoked potential;

Secondary

MeasureTime frame
Surface electromyography;Spinal cord independence measure-3;Modified Barthel Index;Functional near-infrared spectroscopy;

Countries

China

Contacts

Public ContactYuanyuan Chu

Shanghai Hebin Rehabilitation Hospital

751500692@qq.com+86 21 5767 3300

Outcome results

None listed

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