Symptom-driven Referral for Evaluation of Chronic Thromboembolic Disease or Pulmonary Hypertension in Patients With Previous Acute Pulmonary Embolism
1 other identifier
interventional
100
0 countries
N/A
Brief Summary
Aim: To investigate if a symptom driven referral for chronic thrombosis in the lungs after acute pulmonary embolism is better than the current approach. Background: A number of patients with chronic thrombosis in the lungs after acute pulmonary embolism have dyspnea and reduced functional capacity without elevated pulmonary arterial pressure at rest (CTED). However, current guidelines for follow-up after acute pulmonary embolism will miss all patients with CTED, as referral for further examination is based on elevated pulmonary arterial pressure on echocardiography. Thus, the prevalence of CTED is unknown. The hypothesis is, that a symptom-driven referral of patients with previous acute pulmonary embolism is more sensitive in diagnosing CTED than the current approach. Methods and materials: Patients diagnosed with acute pulmonary embolism in Region Midt (approx. 350 per year) will be screened for non-recovery or persistent pulmonary embolism related symptoms during their 3-6 months follow up at their local outpatient clinic. If the patient has persistent symptoms they will be referred to a scintigraphy. If CTED is suspected from the scintigraphy, the patient will be referred for full CTED work-up. The investigators expect to screen 300 patients for persistent symptoms with an expected study time of 3 years.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Feb 2019
Longer than P75 for not_applicable
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
November 1, 2018
CompletedFirst Posted
Study publicly available on registry
November 2, 2018
CompletedStudy Start
First participant enrolled
February 1, 2019
CompletedPrimary Completion
Last participant's last visit for primary outcome
November 1, 2022
CompletedStudy Completion
Last participant's last visit for all outcomes
November 1, 2022
CompletedNovember 2, 2018
October 1, 2018
3.8 years
November 1, 2018
November 1, 2018
Conditions
Outcome Measures
Primary Outcomes (1)
Prevalence of CTED
3 years
Secondary Outcomes (1)
Diagnostic accuracy of dual energy CT perfusion and pulmonary angiography.
3 years
Study Arms (1)
CTEPH/CTED work-up
OTHERInterventions
Patients diagnosed with acute pulmonary embolism (PE) in Region Midt (approx. 350 per year) will be screened for non-recovery or persistent PE related symptoms during their 3-6 months follow up at their local outpatient clinic. If the patient has persistent symptoms they will be referred to a V/Q-scan. If a V/Q mismatch is present, the patient will be referred to a full work-up for CTEPH/CTED.
Eligibility Criteria
You may qualify if:
- Acute PE diagnosed by CT or V/Q-scan within the last year.
- Non-recovery or persistent PE related symptoms assessed by a MRC breathlessness score or WHO functional class.
- Age \>= 18 and \< 80
You may not qualify if:
- Contraindications or unable to perform 6 minutes walk distance (6MWD) and/or cardiopulmonary exercise test.
- Contraindications to CT pulmonary angiography.
- Congestive heart failure (LVEF \<40%).
- COPD or restrictive lung disease, severe or worse (FEV1 \<50% and \>=1 exacerbation causing hospital admission per year (GOLD grade 3 and 4 class C and D)).
- Lactating or pregnant.
- Unable or unwilling to provide written informed consent.
- Paroxysmal or persistent atrial fibrillation.
- Other known cause of PE related symptoms.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- University of Aarhuslead
- Hospitalsenheden Vestcollaborator
Study Officials
- STUDY CHAIR
Asger Andersen, MD, PhD
Aarhus University Hospital
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- DIAGNOSTIC
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
November 1, 2018
First Posted
November 2, 2018
Study Start
February 1, 2019
Primary Completion
November 1, 2022
Study Completion
November 1, 2022
Last Updated
November 2, 2018
Record last verified: 2018-10
Data Sharing
- IPD Sharing
- Will not share