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Clinical Trials/KCT0007126
KCT0007126
Recruiting
未知

Influencing factors for surgical outcomes on anterior cervical discectomy and fusion (ACDF) using allo-bone grafts – Prospective, single arm, multi-center study

Kyung Hee University Hospital0 sites100 target enrollmentTBD
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ConditionsDiseases of the musculoskeletal system and connective tissue

Overview

Phase
未知
Intervention
Not specified
Conditions
Diseases of the musculoskeletal system and connective tissue
Sponsor
Kyung Hee University Hospital
Enrollment
100
Status
Recruiting
Last Updated
4 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
4 years ago
Study Type
Observational Study
Sex
All

Investigators

Sponsor
Kyung Hee University Hospital

Eligibility Criteria

Inclusion Criteria

  • •Patients with neurological symptoms due to cervical myelopathy or neuromuscular disease
  • •\- Patients who have been diagnosed with cervical myelopathy or neuromuscular disease and have no improvement in symptoms despite active conservative treatment for more than 3 months
  • •\- Patients undergoing surgery using allograft during anterior fusion
  • •\- Adults between 20 and 80 years of age
  • •\- Patients who are able to express their pain or dysfunction and consent to the preoperative study

Exclusion Criteria

  • •\- Patients with a history of previous cervical spine surgery
  • •\- Patients who need posterior surgery in addition to anterior surgery
  • •\- Patients with other underlying diseases other than cervical myelopathy or neuromuscular disease that may cause upper extremity sensorine abnormalities and affect outcome evaluation.
  • •ex) Tumor, Carpal tunnel syndrome, cubital tunnel syndrome, Parkinson’s disease, Amytrophic lateral sclerosis
  • •\- Adolescents under the age of 20 or elderly patients over 80 years of age
  • •\- Patients who are medically incapable of consenting or unable to communicate
  • •\- Women who are pregnant, lactating, or planning to become pregnant during the study period

Outcomes

Primary Outcomes

Not specified

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