Pulmonary Embolism Short-term Clinical Outcomes Registry
| Status: | Recruiting |
|---|---|
| Conditions: | Cardiology, Cardiology |
| Therapuetic Areas: | Cardiology / Vascular Diseases |
| Healthy: | No |
| Age Range: | 18 - Any |
| Updated: | 7/21/2018 |
| Start Date: | August 2016 |
| End Date: | March 2020 |
| Contact: | Anthony Weekes, MD |
| Email: | anthony.weekes@carolinashealthcare.org |
| Phone: | 704-355-3181 |
Pulmonary Embolism Short-term Clinical Outcomes Registry (PE-SCOR)
The overall goal of this clinical research study is to prospectively assess primary outcomes
related to pulmonary embolism (PE) that occur immediately (within 5 days) and within 30 days.
The secondary goal is to compare validated prediction models and a modified European Society
of Cardiology (ESC) approach that is primarily right ventricle dysfunction (RVD) driven with
clinical risk assessment being secondary, and with primary outcomes of clinical deterioration
within 5 days.
related to pulmonary embolism (PE) that occur immediately (within 5 days) and within 30 days.
The secondary goal is to compare validated prediction models and a modified European Society
of Cardiology (ESC) approach that is primarily right ventricle dysfunction (RVD) driven with
clinical risk assessment being secondary, and with primary outcomes of clinical deterioration
within 5 days.
The investigators wish to develop the Pulmonary Embolism Short-term Clinical Outcomes
Registry (PE-SCOR). The investigators also wish to determine the incidence of death and
circulatory and respiratory deterioration, and administration of reperfusion therapy within 5
days in PE patients. The study will also evaluate the sensitivity, specificity and positive
and negative predictive values of each RVD assessment option. The investigators will also
derive a prediction model for PE patients for the primary outcome within five days. Finally,
investigators will determine the functional outcomes of PE patients 30 days after PE.
Registry (PE-SCOR). The investigators also wish to determine the incidence of death and
circulatory and respiratory deterioration, and administration of reperfusion therapy within 5
days in PE patients. The study will also evaluate the sensitivity, specificity and positive
and negative predictive values of each RVD assessment option. The investigators will also
derive a prediction model for PE patients for the primary outcome within five days. Finally,
investigators will determine the functional outcomes of PE patients 30 days after PE.
Inclusion Criteria:
- Patients 18 years or older with image confirmed acute pulmonary embolism diagnosed
within 12 hours of ED presentation will be eligible for enrollment.
Exclusion Criteria:
- Patients who refuse consent for 30-day clinical contact and follow-up.
We found this trial at
7
sites
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Charlotte, North Carolina 28203
Principal Investigator: Anthony Weekes, MD
Phone: 704-620-2950
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