About this trial
The goal of this study is to explore the indications and application scope of spinal endoscopy combined with annulus fibrosus repair technology, with a focus on verifying the effectiveness of annulus fibrosus suture technology and evaluating its safety, so as to further support the promotion of annulus fibrosus repair technology in patients with lumbar disc herniation.
Eligibility criteria
Qualifiers
Age: 12 years old to 65 years old, gender not limited;
Diagnosed with Lumbar disc herniation;
Preoperative intervertebral disc MRI Pfirrmann grade I - II;
Conservative treatment is ineffective, and the symptoms significantly affect life;
Disqualifiers
Accompanied by lumbar spondylolisthesis, lumbar instability and other lumbar diseases, etc.
Previous history of lumbar spine surgery;
Those who have other major physical diseases and are unable to tolerate surgery;
Diseases such as malnutrition, abnormal bone metabolism, and autoimmune diseases that may affect the postoperative development process;
Trial design
Treatments tested in this trial
- Repair of the annulus fibrosus
Treatment groups
Sponsors and collaborators
The Affiliated Hospital of Qingdao University
Lead sponsor
Qilu Hospital of Shandong University
Collaborator
Shandong Provincial Hospital
Collaborator
Qianfoshan Hospital
Collaborator
Peking Union Medical College Hospital
Collaborator
First Affiliated Hospital of Harbin Medical University
Collaborator
First Affiliated Hospital of Wenzhou Medical University
Collaborator
The Fourth Affiliated Hospital of Zhejiang University School of Medicine
Collaborator
The Third Xiangya Hospital of Central South University
Collaborator
Second Affiliated Hospital of Xi'an Jiaotong University
Collaborator