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NCT04411888 Clinical Trial

Pulmonary Embolism Prognosis Model

Pulmonary Embolism Clinical Trial

Official title:
Observation Study of Clinical Manifestation and Outcome in Chinese Pulmonary Embolism

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT04411888
Other study ID # PUMCH--Pulmonary embolism
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date June 1, 2020
Est. completion date June 1, 2024

Study information
Verified date May 2020
Source Peking Union Medical College Hospital
Contact Juhong Shi, M.D
Phone +8613701178492
Email shijh@pumch.cn
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The purpose of this study is to analyze the clinical manifestations, imaging features, and prognosis-related factors of pulmonary embolism, and to explore the prognosis risk assessment model for Chinese patients

Description:

Patients with pulmonary embolism and aged 18 years or older were enrolled in this study.Patient demographic characteristics((age, sex, department, diagnosis, ), basic vital signs, symptoms at their admissions (hemoptysis, dyspnea, chest pain, syncope), laboratory examinations (blood lab routines, blood gas, liver and kidney function, myocardial marker), and imaging examinations (vascular ultrasonography, computed tomographic angiography, echocardiography, chest CT, CTPA, pulmonary perfusion imaging, pulmonary angiography, PET/CT) were collected by reviewing the cases. The prognostic information was collected by telephone follow-up. The follow-up end point was June 2024.

Recruitment information / eligibility
Status Recruiting
Enrollment 1500
Est. completion date June 1, 2024
Est. primary completion date June 1, 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years to 90 Years
Eligibility Inclusion Criteria:

Aged 18 years or older. Discharged with the diagnosis of PE from Peking Union Medical College Hospital.

Exclusion Criteria:

Diagnosed PE by other health care facility or transferred from other health care facility .

Without important follow-up data.

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• observation
observation

Locations
Country Name City State
China Peking Union Medical College Hospital Beijing Beijing

Sponsors (1)
Lead Sponsor Collaborator
Peking Union Medical College Hospital

Country where clinical trial is conducted

China, 

Outcome
Type Measure Description Time frame Safety issue
Primary Patient survival time Patient survival time after diagnosed as pulmonary embolism Through study completion, an average of 4 year
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