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Clinical Trial Summary

The purpose of this trial was to investigate the safety and efficacy of fuser lateral bone grafting in ACDF. By observing the intervertebral bony fusion rate and clinical outcome scores of patients after fusion device lateral bone grafting, it was verified whether the fusion device lateral bone grafting approach could improve the bony fusion rate and clinical outcome of ACDF.


Clinical Trial Description

The study will include patients who underwent 1-2 segment ACDF surgery, in addition to conventional surgical operations, the appropriate amount of allograft bone was implanted in the joint space of the hook vertebrae lateral to the fusion device, and X-rays and CTs were reviewed in the immediate postoperative period, March, June, and December, to verify intervertebral osseous fusion, as well as to observe the patient's clinical outcomes. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06027827
Study type Observational
Source Xuanwu Hospital, Beijing
Contact Fengzeng Jian, MD, PhD
Phone 135 5206 7268
Email fengzengjian@hotmail.com
Status Recruiting
Phase
Start date December 1, 2022
Completion date December 2024

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