Comparative study of clinical and radiological outcomes of anterior cervical discectomy and fusion using ceramic cage or PEEK cage: a prospective randomized controlled trial.

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

CRIS

Registry ID

KCT0009673

Enrollment

Registered

2024-08-02

Start date

2024-07-02

Completion date

Unknown

Last updated

2024-08-19

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

Conditions

None listed

Interventions

Medical Device : This study evaluates efficacy by analyzing the difference between the use of allogeneic bone grafts and the use of ceramic cages using a randomized method for patients undergoing cerv

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: ? Symptoms and signs of radiation to one or both arms (pain, dyspnea, or paralysis according to the distribution of a particular neuromuscular muscle) or symptoms and signs related to acute or chronic spinal cord disease ? At least 8 weeks of conservative treatment (physical therapy, pain medication) ? Imaging diagnoses of cervical intervertebral valve dislocation and (or) osteoclastic formation in one or two segments associated with clinical symptoms and signs (from cervical spine 3-4 to cervical spine 7 to thoracic spine 1) are possible ? who want to participate in clinical research ? with prior written consent from the patient or his/her legal representative

Exclusion criteria

Exclusion criteria: ? Uncertain or ambiguous symptoms ? previous history of anterior or posterior access cervical spine surgery ? If there is a risk of instability due to a height difference of more than 3 mm in simple radiographic examination of extension and flexion ? Severe post-chronic symptoms in the segment (above 7 degrees) ? Patient fails to take MRI ? Who has cervical pain without radiating symptoms or spondylosis ? In the presence of an infectious disease ? In the case of metabolic diseases such as severe osteoporosis or bone diseases ? Who has a tumor or trauma to your cervical spine ? Who has deformity of the spine ? Who has a severe mental illness

Design outcomes

Primary

Measure	Time frame
Change in VAS(Visual Analogue Scale), Change in K-NDI	—

Secondary

Measure	Time frame
Radiologic evaluation	—

Countries

Korea, Republic of

Contacts

Public ContactCho-rong Lee

The Catholic University of Korea, Seoul St. Mary's Hospital

chorong1984@gmail.com+82-2-2258-6844

Outcome results