ClinicalTrials.Veeva

Menu

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

P

Peking University

Status

Completed

Conditions

Cervical Myelopathy
Ossification of Posterior Longitudinal Ligament in Cervical Region

Treatments

Procedure: Intensive recovery management

Study type

Observational

Funder types

Other

Identifiers

NCT04947891
M2017310

Details and patient eligibility

About

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.

Full 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.

Enrollment

130 patients

Sex

All

Ages

17 to 80 years old

Volunteers

No Healthy Volunteers

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.

Trial design

130 participants in 2 patient groups

Study group
Description:
Patients will be treated with intensive recovery method after surgery.
Treatment:
Procedure: Intensive recovery management
Control group
Description:
Patients will be treated with regular recovery method after surgery.

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems