- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05867732
A Multicenter Observational Cohort of Degenerative Spine Diseases in China(DSDC) (DSDC)
May 19, 2023 updated by: Wenle Li, Xiamen University
A Multicenter Observational Cohort of Degenerative Spine Diseases in China
Study type: The objectives of this observational study were to understand, analyze, and compare the treatment and prognosis of patients with degenerative spine diseases and to construct a risk warning model and an assisted decision-making system
The main questions it aims to answer are:
- [question 1] to construct a database of patients with degenerative spinal diseases and to study their associated prognosis, complications, and other risks
- [Question 2] Use big data to build a risk early warning model and assisted decision making system The study will not intervene with patients
Study Overview
Status
Completed
Conditions
Study Type
Observational
Enrollment (Actual)
10000
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
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Xianmen, China, 361102
- Wenle Li
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Sampling Method
Non-Probability Sample
Study Population
Patients with degenerative spine disease (lumbar disc herniation, lumbar spinal stenosis, lumbar spondylolisthesis, scoliosis deformity, etc.) seen and treated in participating units between January 2015 and January 2022, excluding patients with neoplastic disease
Description
Inclusion criteria:
- patients with degenerative spine disease admitted to the units participating in the study from January 2015 to mid-January 2022;
- complete patient data with no more than 5% missing;
Exclusion Criteria:
- Patients with oncology;
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Collect demographics (Hospital Information System)
Time Frame: 2022.03
|
Collect demographics from the HIS system for patients with degenerative spine disease
|
2022.03
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Wenle Wenle, M.D., Xiamen University
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
March 1, 2022
Primary Completion (Actual)
March 10, 2022
Study Completion (Actual)
March 1, 2023
Study Registration Dates
First Submitted
May 11, 2023
First Submitted That Met QC Criteria
May 19, 2023
First Posted (Actual)
May 22, 2023
Study Record Updates
Last Update Posted (Actual)
May 22, 2023
Last Update Submitted That Met QC Criteria
May 19, 2023
Last Verified
May 1, 2023
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- XiamenUDSDC
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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