CompletedNot Applicable

The Establishment of the Integration of Surgery and Postoperative Intensive Recovery of Patients With CSM

China130 participantsStarted 2017-12-06

Plain-language 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.

Who can participate

Age range17 Years – 80 Years

SexALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * (1) Age: 18\~70 years. (2) Diagnosed as CSM or OPLL. (3) Going to receive C3-C7 open-door laminoplasty. (4) Agree to join this study and sign the informed consent. Exclusion Criteria: * (1) Anterior and posterior combined surgery. (2) Posterior laminoplasty combined fusion. (3) Severe osteoporosis. (4) Morbid obesity. (5) patients with mental disorder. (6) patients with previous history of cervical spine surgery. (7) Abnormal laboratory report of liver function, kidney function and hematologic system.(8) Poor compliance. (9) Patients with other surgical contraindications. (10) Patients with intemperance or taking drugs. (11) Patients who joined other study within the last 3 months.

What they're measuring

Cervical spine mechanical analysis

Timeframe: Preoperation to 1 year after surgery.

Cervical spine functions

Timeframe: Preoperation to 1 year after surgery.

Trial details

NCT IDNCT04947891

SponsorPeking University Third Hospital

Sponsor typeOTHER

Study typeOBSERVATIONAL

Primary completion2020-06-15

View on ClinicalTrials.gov More Cervical Myelopathy trials