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A prospective study for the effects of Improved Contralateral Seventh Cervical Nerve Transfer for Spastic Arm Paralysis

A prospective study for the effects of Improved Contralateral Seventh Cervical Nerve Transfer for Spastic Arm Paralysis

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000029319
Enrollment
Unknown
Registered
2020-01-24
Start date
2020-02-01
Completion date
Unknown
Last updated
2020-02-03

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

Conditions

Spastic limb paralysis after central nervous system injury

Interventions

Group 1:improved contralateral seventh cervical nerve transfer with conventional rehibilitation
Group 2:conventional contralateral seventh cervical nerve transfer with conventional rehibilitation

Sponsors

Department of Burns and Plastic Surgery, Affiliated Hospital of Zunyi Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
12 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Spastic hemiplegia following different causes of central neurologic injury, such as stroke, traumatic brain injury, and cerebral palsy,majorly presenting but not limited to difficulty in hand-open; 2. Aged 45-65 years old; 3. At least one year and no more than 5 years, after sick . The patients have received regular rehabilitation therapy for at least 6 months, and ceased improving in the paralyzed hand; 4. Central neurologic injury only involving the hemisphere contralateral to the paralyzed hand, as indicated by brain MRI scans; 5. The paralyzed hand is controlled by the ipsilesional hemisphere exclusively, as indicated by transcranial magnetic stimulation (TMS); 6. Willing (or their parents were willing if the patients were underage) to receive surgeries to achieve further functional improvement; 7. The patients can fully understand and agree to the doctor's treatment plan and sign an informed consent form.

Exclusion criteria

Exclusion criteria: 1. Central nervous system damage involving both hemispheres of the brain; 2. Presence of severe, deformity or joint contracture; 3. Main presentation is ankylosis of joints; 4. Presence of severe systemic diseases such as diabetes mellitus or cardiopulmonary diseases,contraindicating surgery; 5. Personal or relatives decision to refuse surgery; 6. Psychological or mental abnormalities; 7. Developmental delay or low cognitive ability.

Design outcomes

Primary

MeasureTime frame
total score change of upper limb Fugl-Meyer scale;

Secondary

MeasureTime frame
total score change of upper limb improved Ashworth scale;Functional Use;Neurological electrophysiology;functional MRI;Muscle strength;Tactile sensation;two-point discrimination;

Countries

China

Contacts

Public ContactZairong Wei

Affiliated Hospital of Zunyi Medical University

188116999@qq.com+86 15208660008

Outcome results

None listed

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