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Application of MUNIX in evaluating the surgical effect of patients with cervical spondylosis muscular atrophy

Application of MUNIX in evaluating the surgical effect of patients with cervical spondylosis muscular atrophy

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1800019722
Enrollment
Unknown
Registered
2018-11-25
Start date
2018-12-01
Completion date
Unknown
Last updated
2018-12-04

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

Conditions

Cervical Spondylotic Amyotrophy

Interventions

proximal CSA patients:operation
distal CSA patients:operation
normal control:non-operation

Sponsors

Huashan Hospital, Fudan University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: The criteria for CSA diagnosis: (1) the presence of cervical spondylosis supported by radiological evidence; (2) unilateral or bilateral severe muscle atrophy of the upper extremities; (3) mild or no sensory deficit in the upper extremities; (4) normal sensation and motor function of the lower extremities, without gait disturbance; (5) minimal or no radiative pain of the upper limbs.

Exclusion criteria

Exclusion criteria: (1) history of syringomyelia or spinal cord tumour; (2) other focal or multifocal neuropathy; (3) brachial plexus injury; (4) congenital muscular dystrophy; (5) Hirayama disease; (6) primary or concomitant neuromuscular junction diseases; (7) concomitant trauma, inflammation or infection.

Design outcomes

Primary

MeasureTime frame
MUNIX;handgrips;MMT;

Contacts

Public ContactZheng Chaojun

Huashan Hospital, Fudan University

countd2388@163.com+86 13564635319

Outcome results

None listed

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