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Clinical Trial Summary

This study aims to establish the specialist consensus of the integration of posterior approach surgical treatment and postoperative intensive recovery management for CSM or OPLL patients, and verify its safety, practicability and reliability.


Clinical Trial Description

In order to establish the specialist consensus of the integration of posterior approach surgical treatment and postoperative intensive recovery management, and verify its safety, practicability and reliability, this study enrolled 130 patients with CSM or OPLL undergoing C3-7 open-door laminoplasty. Patients are divided in two groups randomly. The study group has 80 patients, treated with postoperative intensive recovery management, and the control group has 50 patients. The data is collected preoperatively, at 3-month follow-up and 1-year follow-up. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04947891
Study type Observational
Source Peking University Third Hospital
Contact
Status Completed
Phase
Start date December 6, 2017
Completion date December 20, 2020

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