Creating a database for acute osteoporosis vertebral compression fractures
The Construction of Bidirectional Column Study and Prognosis Prediction of Acute Osteoporotic Vertebral Compression Fractures Based on Imaging and Clinical Data
This study is trying to create a database to better understand acute osteoporosis-related spine fractures and see how different factors affect recovery for patients.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 500 (estimated) |
| Ages | 50 Years to 100 Years |
| Sex | All |
| Sponsor | Peking University Third Hospital Academic / other |
| Locations | 1 site (Beijing) |
| Trial ID | NCT06586996 on ClinicalTrials.gov |
What this trial studies
This observational study aims to establish a bidirectional cohort focused on predicting the prognosis of acute osteoporotic vertebral compression fractures using both imaging and clinical data. The research will compile a comprehensive bioinformation database that includes patient status, clinical data, laboratory examinations, and imaging results. By analyzing this data, the study seeks to enhance understanding of the condition and improve patient outcomes.
Who should consider this trial
Good fit: Ideal candidates for this study are patients who have suffered from acute osteoporosis vertebral compression fractures.
Not a fit: Patients with endocrine diseases that affect bone density may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could provide valuable insights into the prognosis of patients with acute osteoporotic vertebral compression fractures, leading to better management strategies.
How similar studies have performed: While this approach is focused on establishing a new database, similar studies have shown promise in improving prognosis prediction for osteoporosis-related fractures.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: all patients who suffer a acute osteoporosis vertebral compression fractures - Exclusion Criteria: those who have endocrine disease which have impacts on the bone density -
Where this trial is running
Beijing
- Peking University Third Hospita — Beijing, China (Recruiting)
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.