Clinical Scores, Biomarkers, and CT Findings in Acute Pulmonary Embolism

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorSohag University

About this trial

This study aims to compare clinical scoring systems, laboratory biomarkers, and computed tomography (CT) findings in patients diagnosed with acute pulmonary embolism in different hospital departments.

The study will include patients diagnosed with acute pulmonary embolism at Sohag University Hospital. Clinical data, laboratory results, and imaging findings will be collected and analyzed to evaluate their diagnostic and prognostic value.

The goal of this research is to identify the most reliable and practical tools for early diagnosis and risk stratification of acute pulmonary embolism, which may help improve patient management and outcomes.

This is an observational study and does not involve any intervention or change in standard patient care.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

• Adults aged ≥ 18 years

Confirmed acute pulmonary embolism by CTPA

Disqualifiers

• Chronic pulmonary embolism

Non-diagnostic CTPA

Refusal to participate

Severe renal impairment precluding contrast-enhanced CT

Trial population

Adult patients with confirmed acute pulmonary embolism admitted to Sohag University Hospital from different departments including Emergency, ICU, Medical, and Surgical wards.

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

  • No Intervention (Observational Study Data Collection)

    Other intervention

    This is an observational study with no active intervention. All data are collected from routine clinical care, including clinical scoring systems, laboratory biomarkers, and computed tomography pulmonary angiography (CTPA) findings in patients with acute pulmonary embolism.

Treatment groups

50 Participants
are divided into 1 treatment group
Group A: Acute Pulmonary Embolism Group1 intervention

Trial outcomes

Primary outcomes

1

Number of Participants with In-Hospital All-Cause Mortality

All-cause mortality among adult patients with confirmed acute pulmonary embolism, defined as death from any cause occurring during hospitalization. The outcome will be assessed as the number of participants who die before hospital discharge.

Time frame
Up to 30 days

Secondary outcomes

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

This trial is not recruiting at the moment. You can still explore other options: