Cardiovascular Morbidities and Lung Cancer Treatment: a Prospective Registry
NCT ID: NCT03368820
Last Updated: 2021-08-23
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
200 participants
OBSERVATIONAL
2017-12-04
2023-12-31
Brief Summary
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The aim of this registry is to determine if and how cardiovascular co-morbidities impact on the physicians' decision for anticancer treatment in lung cancer patients by comparing it to the European Lung Cancer Working Party (ELCWP) guidelines
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Interventions
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No intervention
Treatment left at the discretion of the participant
Eligibility Criteria
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Inclusion Criteria
* Untreated lung cancer of any stage and any treatment (including palliative care only).
* Availability for participating in the detailed follow-up of the protocol.
* Signed informed consent.
* Age above 18 years.
* Presence of at least one co-morbidity:
* Any active or past cardiac ischemia
* Reduced left ventricular ejection fraction (\< 50%)
* Obstructive cardiomyopathy
* Valvular dysfunction (3 or 4/4; valvular replacement)
* Arrhythmia (atrial flutter or fibrillation, significant ventricular arrhythmia, 2nd-3rd degree auriculo-ventricular block, Wolf-Parkinson-White and other similar aberrant conduction, bifascicular block, arrhythmogenic right ventricular dysplasia)
* Uncontrolled hypertension (systolic blood pressure (BP) \> 160 millimeter of mercury (mmHg) or diastolic BP \> 100 mmHg on ≥ 1 hypotensive drug) or controlled hypertension on ≥ 2 concurrent hypotensive drugs
* Active or treated peripheral arteritis (grade 2 or more)
* Cerebrovascular events
* Pulmonary embolism and/or thrombophlebitis or patients at high risk of thrombophilia (homozygous Leiden factor…)
* Aortic aneurism
Exclusion Criteria
* Patient previously treated for lung cancer.
* Tumours for which complete staging cannot be assessed.
* History of prior malignant tumour, except non-melanoma skin cancer or in situ carcinoma of the cervix or of the bladder or cured malignant tumour (more than 5-year disease free interval).
18 Years
ALL
No
Sponsors
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European Lung Cancer Working Party
OTHER
Responsible Party
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Principal Investigators
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Thierry Berghmans, MD, PhD
Role: STUDY_CHAIR
ELCWP
Locations
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Department of Intensive Care Unit and Thoracic Oncology Institut Jules Bordet
Brussels, , Belgium
Hôpital Saint-Joseph
Charleroi, , Belgium
CHU Tivoli
La Louvière, , Belgium
Hôpital Ambroise Paré
Mons, , Belgium
CH Peltzer-La Tourelle
Verviers, , Belgium
Hôpital Mont-Godinne
Yvoir, , Belgium
Countries
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Central Contacts
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Facility Contacts
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Thierry Berghmans, MD
Role: primary
Benoit Colinet, MD
Role: primary
Ingrid CsToth, MD
Role: primary
Stéphane Holbrechts, MD
Role: primary
Yves Bonduelle, MD
Role: primary
Sebahat Ocak, MD, PhD
Role: primary
Other Identifiers
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01151
Identifier Type: -
Identifier Source: org_study_id
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