Actively Recruiting
Optimal Time for Reperfusion in Acute Pulmonary Embolism Observational Study
Led by Azienda ULSS 8 Berica · Updated on 2026-03-03
500
Participants Needed
7
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
Pulmonary embolism (PE) is a leading cause of death related to heart and blood vessel problems worldwide. This research aims to understand how the timing of treatments that clear blood clots, such as systemic thrombolysis or catheter-based therapies, affects survival and complications in patients with high-risk or intermediate-high-risk PE. The study seeks to find the best time window for these treatments to improve outcomes, as current guidelines do not specify exact timing. The study is a national, multicenter, prospective observational trial focusing on patients classified as high-risk or intermediate-high-risk PE according to European Society of Cardiology guidelines. It observes the use and timing of reperfusion treatments like systemic thrombolysis or catheter-directed therapies. These treatments are given as needed based on the patient’s condition, with no experimental drug or procedure assigned by the study. Participants will be monitored from enrollment through 30 days of treatment to track survival and any bleeding or heart-related complications. Data will be collected on treatment timing and patient outcomes without altering usual care. This approach helps researchers understand how timing influences the effectiveness and safety of reperfusion therapies in real-world settings.
CONDITIONS
Brief Title
Optimal Time for Reperfusion in Acute Pulmonary Embolism
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age 18 years or older
- Diagnosed with intermediate-high or high-risk pulmonary embolism confirmed by CT pulmonary angiography, pulmonary angiography, or echocardiography
- Classified as high-risk or intermediate-high-risk according to 2019 European Society of Cardiology guidelines
- Provided informed consent for processing of personal data
You will not qualify if you...
- Under 18 years of age
- Diagnosed without acute high-risk or intermediate-high-risk pulmonary embolism
- Unable to provide informed consent
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Up to a few days after screening
Participants diagnosed with intermediate-high or high-risk pulmonary embolism are evaluated to confirm eligibility and classification according to guidelines.
1 to 2 visits depending on diagnostic tests
Duration - Up to 30 days from enrollment
Participants are observed to assess timing and outcomes of systemic reperfusion or catheter-directed therapies when indicated, focusing on in-hospital mortality and complications.
Hospital visits as part of routine care during the 30-day period
Trial Site Locations
Total: 7 locations
1
UO Unità di Cure Intensive Cardiologiche e Cardiologia 1, Ospedale Niguarda, Milano
Milan, Milano, Italy, 20162
Actively Recruiting
2
UOC di Cardiologia, Ospedali Riuniti Padova Sud, Monselice, Italia
Monselice, Padova, Italy, 35043
Actively Recruiting
3
IRCCS Policlinico San Matteo
Pavia, Pavia, Italy, 27100
Actively Recruiting
4
UO di Sezione di Medicina Interna e Cardiovascolare, Ospedale Santa Maria della Misericordia, Perugia, Italia
Perugia, Perugia, Italy, 06129
Actively Recruiting
5
UO di Cardiologia 1, Azienda Ospedaliero Universitaria Pisana, Pisa, Italia
Pisa, Pisa, Italy, 56126
Actively Recruiting
6
UO di Cardiologia, Azienda Ospedaliera Ordine Mauriziano di Torino
Torino, Torino, Italy, 10128
Actively Recruiting
7
UOC di Cardiologia, Ospedali dell'Ovest Vicentino, Arzignano, IItalia
Arzignano, Vicenza, Italy, 36071
Actively Recruiting
Research Team
C
Claudio Bilato, MD PhD
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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