A system to prevent blood clots during surgery using big data analysis
Construction of Perioperative Venous Thromboembolism Risk Prevention System Based on Big Data Analysis and Multimodule System
Shengjing Hospital · NCT05969951
This study is trying to create a new system using big data to help prevent blood clots during and after surgery for patients aged 10 to 90.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 100000 (estimated) |
| Ages | 10 Years to 90 Years |
| Sex | All |
| Sponsor | Shengjing Hospital (other) |
| Locations | 1 site (Shenyang, Liaoning) |
| Trial ID | NCT05969951 on ClinicalTrials.gov |
What this trial studies
This observational study aims to develop a comprehensive and reliable risk prevention system for venous thromboembolism (VTE) during the perioperative period by utilizing medical big data and a multi-module computer approach. VTE, which includes deep vein thrombosis (DVT) and pulmonary thromboembolism (PTE), is a significant cause of postoperative complications and mortality. The study will assess perioperative patients aged 10 to 90 years, gathering data to improve risk assessment and prevention strategies. By enhancing the existing Caprini scale, the study seeks to adapt to modern surgical practices and patient profiles.
Who should consider this trial
Good fit: Ideal candidates for this study are perioperative patients aged 10 to 90 years who can provide informed consent.
Not a fit: Patients who have already developed DVT or pulmonary embolism prior to surgery or those undergoing emergency operations may not benefit from this study.
Why it matters
Potential benefit: If successful, this system could significantly reduce the incidence of VTE and related mortality in perioperative patients.
How similar studies have performed: Previous studies have shown success in using risk assessment scales like the Caprini scale, but this approach aims to innovate and adapt to current clinical practices.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: 1. perioperative patients; 2. Age range from 10 to 90 years old, gender unlimited; 3. Sign informed consent. Exclusion Criteria: * (1) non-operative patients; (2) have developed deep vein thrombosis and/or pulmonary embolism before surgery; (3) emergency operation patients; (4) Patients considered unsuitable for inclusion in the study.
Where this trial is running
Shenyang, Liaoning
- Shengjing Hospital of China Medical University — Shenyang, Liaoning, China (RECRUITING)
Study contacts
- Study coordinator: Chuming Zhou, master
- Email: zcm_06@163.com
- Phone: +8602496615-21111
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.
Conditions: Recruiting