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Real World Data Collection and Analysis on the Anterior Cervical Spine Surgery (ACCSS)

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Capital Medical University

Status

Enrolling

Conditions

Cervical Disc Degeneration

Treatments

Other: Collection Data

Study type

Observational

Funder types

Other

Identifiers

NCT05602714
KY201402502

Details and patient eligibility

About

This observational study aims to evaluate the efficacy and safety of anterior cervical spine surgery in patients with cervical degenerative disc disease

Full description

This observational study is an ambispective cohort designed. Patients who are diagnosed cervical degenerative disc disease will be selected to join in this study. Visual Analogue Scale, Japanese Orthopaedic Association Scale, Neck Disability Index, SF-36, and device related or procedure related adverse events will be recorded and compared to evaluate the efficacy and safety of anterior cervical spine surgery in patients with cervical degenerative disc disease

Enrollment

1,500 estimated patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Patients over 18 years old
  2. Clinical symptoms and imaging support cervical degenerative disc disease;
  3. Failed a minimum of 3months conservative treatment
  4. Have had (retrospective cohort) or the decision has been made to have (prospective cohort) anterior cervical spine surgery
  5. Written informed consent given by subject

Exclusion criteria

  1. Patients with non-degenerative (e.g., trauma, tumor, and infection) or neuromuscular diseases (e.g., motor neuron disease) were excluded
  2. Patients with cervical spine X-ray film and CT scan contraindications
  3. Women who are lactating and pregnant

Trial contacts and locations

1

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Central trial contact

Bingxuan Dr. Wu, PhD

Data sourced from clinicaltrials.gov

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