Pulmonary Embolism WArsaw REgistry

Status: Recruiting
Location: See location...
Study Type: Observational
SUMMARY

Initiated in January 2008, The PE-aWARE (Pulmonary Embolism WArsaw REgistry) is an on-going single-centre prospective observational study of patients with confirmed acute pulmonary embolism (APE). Extensive data on consecutive patients with pulmonary embolism is collected and stored. The main objective is to collect and provide information on patients' characteristics, management, and outcome with the purpose of decreasing mortality in APE, the occurrence of bleeding, and the frequency of thromboembolic recurrences. Moreover, the PE-aWARE registry serves as a basis for creating predictive scores for clinicians which aid patient management. The study endpoints comprise clinically recognized (and objectively confirmed) recurrences of PE, major and minor bleeding complications classified according to the International Society on Thrombosis and Haemostasis classification, need for cardiopulmonary resuscitation or catecholamines, and death.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• objectively confirmed pulmonary embolism

• Informed consent for the participation in the study, according to the requirements of the ethics committee

Locations
Other Locations
Poland
Department of Internal Medicine & Cardiology with the Centre for Management of Venous Thromboembolic Disease, Medical University of Warsaw
RECRUITING
Warsaw
Contact Information
Primary
Piotr Pruszczyk, Prof.
piotr.pruszczyk@wum.edu.pl
00 48 22 502 11 44
Backup
Marta Z Skowronska, MD
marta.z.kozlowska@gmail.com
00 48 22 502 16 25
Time Frame
Start Date: 2008-01-01
Estimated Completion Date: 2028-12-31
Participants
Target number of participants: 1500
Treatments
Complicated outcome
The patients meet at least one of the following criteria:~1. systolic blood pressure \< 90 mmHg for at least 15 minutes~2. need for catecholamine administration because of persistant arterial hypotension or shock~3. need for mechanical ventilation~4. need for cardiopulmonary resuscitation~5. bleeding classified according to the International Society on Thrombosis and Haemostasis classification (major bleeding and non-major clinically relevant bleeding).
Non-complicated outcome
The patients meet none of the following criteria:~1. systolic blood pressure \< 90 mmHg for at least 15 minutes~2. need for catecholamine administration because of persistant arterial hypotension or shock~3. need for mechanical ventilation~4. need for cardiopulmonary resuscitation~5. bleeding classified according to the International Society on Thrombosis and Haemostasis classification (major bleeding and non-major clinically relevant bleeding).
Related Therapeutic Areas
Sponsors
Leads: Medical University of Warsaw

This content was sourced from clinicaltrials.gov