Quick Recognition of Aortic Dissection
Recruiting
- Conditions
- Aortic Dissection
- Registration Number
- NCT05699395
- Lead Sponsor
- Shanghai Zhongshan Hospital
- Brief Summary
This is an observational study that establishes a cohort of patients with high risk chest pain who have been identified by CTA for aortic dissection. We then used this cohort to validate the accuracy of identifying aortic dissection based on extremity oximetry and Doppler waveforms.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- All
- Target Recruitment
- 600
Inclusion Criteria
- High risk chest pain with CTA
Exclusion Criteria
- shock
- coma
- severe peripheral vascular diseases
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Diagnosis of aortic dissection First 24-hours during emergency dapartment stay aortic dissection confirmed by CTA
- Secondary Outcome Measures
Name Time Method
Related Research Topics
Explore scientific publications, clinical data analysis, treatment approaches, and expert-compiled information related to the mechanisms and outcomes of this trial. Click any topic for comprehensive research insights.
What molecular mechanisms underlie aortic dissection detection using Doppler waveforms and oximetry?
How does extremity oximetry compare to CTA in diagnosing aortic dissection in high-risk chest pain patients?
What biomarkers are associated with aortic dissection that could enhance patient selection for waveform-based diagnostics?
What are the potential false positive/negative rates of using Doppler and oximetry for aortic dissection detection?
Are there alternative non-invasive diagnostic approaches for aortic dissection compared to NCT05699395's methods?
Trial Locations
- Locations (1)
Zhongshan Hospital, Fudan University
🇨🇳Shanghai, China
Zhongshan Hospital, Fudan University🇨🇳Shanghai, ChinaJingchao Luo, MDContact13121021484sucapter@163.com