Short-term Clinical Deterioration After Acute Pulmonary Embolism

Completed

Conditions studied: Pulmonary Embolism

In brief

This is a prospective, observational, multicenter cohort study to compare right ventricular dysfunction dependent and independent prognostic models for short-term serous adverse events in patients who are diagnosed with pulmonary embolism in the emergency department. Clinical endpoints are assessed at days 1-5. A thirty-day follow-up phone call is conducted to obtain further clinical endpoints and a quality of life assessment.

Key facts

Study ID
NCT03915925
Run by
Wake Forest University Health Sciences
People needed
935
Starts
2018-09-30
Expected to finish
2020-11-30
Last updated by the study team
2022-04-27

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

You may not qualify if…

Where it is running

Full record on ClinicalTrials.gov

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