Actively Recruiting

Age: 18Years +
All Genders
ID07491094

Repeated Examinations for Typing Pulmonary Embolism (RE-TyPE)

Led by Sahlgrenska University Hospital · Updated on 2026-04-06

400

Participants Needed

3

Research Sites

104 weeks

Total Duration

On this page

Sponsors

S

Sahlgrenska University Hospital

Lead Sponsor

G

Gothia Forum - Center for Clinical Trial

Collaborating Sponsor

AI-Summary

What this Trial Is About

Researchers are studying pulmonary embolism (PE), a serious heart and lung condition, focusing on patients with intermediate-high risk PE. The study aims to better understand the early course of this condition and how changes in tests like biomarkers, ECG, and echocardiography during the first 48 hours relate to patient outcomes. It also seeks to create a long-term follow-up system for all PE patients treated at Sahlgrenska University Hospital to improve care quality and outcomes. The study has two parts: Cohort A includes hospitalized patients with intermediate-high risk PE who undergo repeated tests and monitoring during the first three days after diagnosis, including vital signs, echocardiography, ECG, blood tests, and oxygen or circulatory support if needed. Cohort B includes all PE patients diagnosed at the hospital, who are followed over time with baseline and follow-up assessments at about 90 days and beyond 12 months. Cohort B patients not in Cohort A mainly have baseline and longer-term data collected. Participants will have repeated examinations during hospital stays and outpatient visits, including echocardiography and ECG. Researchers will collect clinical data, laboratory samples, and measure outcomes such as clinical deterioration and bleeding within 7 days, plus longer-term outcomes like recurrence of PE, quality of life, and chronic complications. The study will follow patients up to a year or more to assess these outcomes and improve future PE care.

CONDITIONS

Brief Title

Repeated Examinations for Typing Pulmonary Embolism

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adult patients (18 years or older) diagnosed with or followed for pulmonary embolism at Sahlgrenska University Hospital
  • Able to provide written informed consent
Not Eligible

You will not qualify if you...

  • Patients with low risk, intermediate-low risk, or high risk pulmonary embolism (not intermediate-high risk)
  • More than 48 hours have passed since hospital arrival for pulmonary embolism
  • Expected inability to comply with the study protocol (for example, due to dementia)

AI-Screening

AI-Powered Screening

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Your Study Journey

Screening

Duration - Up to 48 hours from pulmonary embolism event

Participants are screened for eligibility to participate in the trial.

1 screening and enrollment visit (in-person)

Monitoring

Duration - Day 0 to Day 2

Participants with intermediate-high risk pulmonary embolism undergo serial clinical examinations including vital signs, ECG, echocardiography, biomarkers, and other assessments during their hospital stay to characterize the early clinical course of pulmonary embolism.

3 visits (in-person) on Day 0, Day 1, and Day 2

Follow-up

Duration - Up to more than 12 months

Participants are followed up to assess clinical outcomes and patient-reported measures at intermediate and long-term timepoints after initial diagnosis or hospitalization.

Visits at approximately Day 30, Day 90, and beyond 12 months (in-person or outpatient)

Trial Site Locations

Total: 3 locations

1

Sahlgrenska University Hospital/Mölndal

Gothenburg, Region Västra Götaland, Sweden

Not Yet Recruiting

2

Sahlgrenska University Hospital/Sahlgrenska

Gothenburg, Region Västra Götaland, Sweden

Actively Recruiting

3

Sahlgrenska University Hospital/Östra

Gothenburg, Region Västra Götaland, Sweden

Not Yet Recruiting

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Research Team

R

Rickard Zeijlon, MD, PhD

M

Mazdak Tavoly, 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

2

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