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Pulmonary Embolism Registry

Pulmonary Embolism Registry

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05391646
Acronym
PER
Enrollment
500
Registered
2022-05-26
Start date
2023-10-31
Completion date
2026-06-16
Last updated
2023-10-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pulmonary Embolism

Keywords

Pulmonary Embolism, Venous Thromboembolism, Chronic Thromboembolic Disease

Brief summary

Acute Pulmonary Embolism (PE) is the most serious clinical presentation of venous thromboembolism (VTE), a leading cause of cardiovascular mortality, exceeded only by stroke and myocardial infarction. Chronic thromboembolic pulmonary hypertension (CTEPH) is the most severe chronic form of CTED and it occurs in 2-4% of patients after acute PE. In Portugal little is known about PE epidemiology and its outcomes, including complications like CTED. The main goal of this study is, therefore, to understand PE epidemiology and complications in the northern region of Portugal. This information can enable the organization of a structured health care network that can potentially benefit all PE patients.

Interventions

None listed

Sponsors

Unidade Local de Saúde de Matosinhos, EPE
CollaboratorOTHER
Centro Hospitalar Universitário do Porto
CollaboratorUNKNOWN
Centro Hospitalar de Vila Nova de Gaia/Espinho, E.P.E.
CollaboratorOTHER_GOV
Hospital da Luz, Portugal
CollaboratorOTHER
Hospital Centre Hospitalar de Trás-os-Montes e Alto Douro
CollaboratorOTHER
Hospital de Braga
CollaboratorOTHER
Centro Hospitalar de Entre o Douro e Vouga
CollaboratorOTHER
Unidade Local de Saúde do Alto Minho
CollaboratorOTHER
Universidade do Porto
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Acute symptomatic or asymptomatic PE, * Age \>18 years, * Availability of a minimum data set for PE and a minimum of 3-months follow-up for the primary objective and 36-months for the secondary one. Except for patients who died prior to the 3 or 36 months follow-up.

Exclusion criteria

* Enrolment of the patient in any treatment trial in a blinded fashion, * Lack or withdrawal of patient´s consent.

Design outcomes

Primary

MeasureTime frameDescription
Determine Pulmonary Embolism (PE) prevalence in PortugalFrom date of inclusion until the end of the study currently planned (3 to 5 years)Number cases per year
Identification of Pulmonary Embolism (PE) risk factors and comorbiditiesFrom date of inclusion until the end of the study currently planned (3 to 5 years)Frequency of risk factors and comorbidities
Determine Pulmonary Embolism (PE) clinical management.From date of inclusion until the end of the study currently planned (3 to 5 years)Identification of diagnostic of diagnostic and treatment profile

Secondary

MeasureTime frameDescription
Access incidence rate of Chronic Thromboembolic Disease (CTED) with or without pulmonary hypertension after acute PE.From 6 months after date of inclusion until the end of the study currently planned (2 to 5 years)ratio between the number of patients with CTED with or without pulmonary hypertension and total number of patients with PE

Contacts

Primary ContactCarolina Guedes, MD, PhDc
cncdc@spc.pt(+351) 93 297 06 93
Backup ContactJanete Santos, PhD
investigaclinica@med.up.pt(+351) 225 513 600

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026