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Linking transcriptional profile of nucleus pulposus to clinical phenotype in intervertebral disc degenerative diseases

Linking transcriptional profile of nucleus pulposus to clinical phenotype in intervertebral disc degenerative diseases

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2200066854
Enrollment
Unknown
Registered
2022-12-20
Start date
2022-12-20
Completion date
Unknown
Last updated
2023-05-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

intervertebral disc degenerative diseases

Interventions

Lumbr Cohort:Bulk RNA-seq of nucleus pulposus
Cervical Cohort:Bulk RNA-seq of nucleus pulposus
Lumbr Validation Cohort:Bulk RNA-seq of nucleus pulposus
Cervical Validation Cohort: Bulk RNA-seq of nucleus pulposus

Sponsors

Army Medical Center of PLA
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients who need surgery treatment due to cervical and/or lumbar disc degenerative diseases meet the following criteria: 1) Age = 18 years old, voluntarily participating in this study, and donating the post operation discarded IVD tissues including nucleus pulposus, annulus fibrosus and cartilaginous endplate; 2) IVD tissue samples and clinical related data could be obtained from the subjects, including but not limited to patient epidemiological data, demographic data, clinical symptoms and signs, imaging data, laboratory examination data, histopathology, treatment methods, and other follow-up information; 3) X-ray and MRI examination profiles of cervical or lumbar spine in posterior anterior position, lateral position, and flexion and extension position. And publicly published scRNA-seq data from patients with disc degenerative diseases who met the above criteria were included.

Exclusion criteria

Exclusion criteria: Patients who met any following criteria, were excluded: 1) Infection of the target disc or its adjacent vertebrae; 2) Participating in other studies and affecting the observation of this study; 3) The subjects are not suitable to participate in the study due to high-risk diseases or other special circumstances.

Design outcomes

Primary

MeasureTime frame
nucleus pulposus transcriptome;sagittal spinopelvic parameters;histological classification for intervertebral disc degeneration;Pfirrmann classification of intervertebral disc degeneration;Demographic data;Epidemiological data of intervertebral disc degenerative diseases;

Countries

China

Contacts

Public ContactLiu peng

Army Medical Center of PLA

liupengd@163.com19923257587

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026