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Study of Individualized, Precise and Standardized Cervical Open-door Surgery for Cervical Spinal Stenosis

NCT05786313 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 500

Last updated 2025-04-09

No results posted yet for this study

Summary

To evaluate the safety and effectiveness of individualized, precise and standardized open-door posterior cervical surgery through a single-center, exploratory clinical study, so as to provide a more reliable basis for the treatment of cervical spinal stenosis.

Conditions

  • Cervical Spinal Stenosis
  • Cervical Spinal Cord Injury
  • Individuation
  • Standardization

Interventions

PROCEDURE

Centerpiece titanium plate

All indexes were collected from the patients with Centerpiece titanium plate for internal fixation.

Sponsors & Collaborators

  • Xijing Hospital

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
FACTORIAL

Eligibility

Min Age
28 Years
Max Age
85 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-03-01
Primary Completion
2025-12-31
Completion
2025-12-31

Countries

  • China

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05786313 on ClinicalTrials.gov