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Clinical Trials in Israel / NCT06723795
Active, not recruiting Not applicable

Cardiovascular Assessment and Treatment During COPD Exacerbation to Improve Diagnosis and Outcomes

NCT06723795 · tracked via the Priya Life Science Israel tracker
Phase
Not applicable
Started
2025-03-01
Last updated
2026-08-25

Condition(s) studied

COPD (Chronic Obstructive Pulmonary Disease)Cardiovascular Diseases

Investigational drug(s) / intervention(s)

Cardiologist evaluationPulmonologist evaluation

Cardiologist evaluation: The cardiology consultation will include the following: a structured interview (see Appendix A), physical examination, review of laboratory tests including HbA1c, lipid profile, BNP, ECG, and POCUS (point-of-care ultrasound) to assess heart contraction and valve function.

Pulmonologist evaluation: optimize basic treatment, and recommend continued follow-up as needed.

Study summary

This is a research study involving patients hospitalized for COPD flare-ups. Patients will be assigned using a non-randomized, sequential allocation strategy (a control cohort followed by an intervention cohort) to two groups: one group will only see a pulmonologist (lung doctor), and the other group will also be seen by a cardiologist (heart doctor) during their hospital stay. Both groups will fill out a questionnaire, and the pulmonologist will review their lung disease, adjust their treatment, and recommend follow-up care. The cardiologist will also assess the second group for heart diseases (like high cholesterol, diabetes, heart disease, high blood pressure, or heart failure) and start or adjust heart treatment if needed. Both groups will be followed up by phone 1, 3, 6 and 12 months later to check for changes in treatment, new heart problems, COPD flare-ups, or death.

Eligibility

Sex
ALL
Min age
18 Years
Max age
75 Years
Healthy volunteers
No
Inclusion Criteria: * Documented COPD (based on lung function tests, symptoms and relevant treatment). * Aged 18-75 years. * Mentally competent to understand and follow medical recommendations. Exclusion Criteria: * Under 18 years of age. * Unable to provide consent. * Unstable concurrent disease.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Tel-Aviv Sourasky Medical Center Tel Aviv Israel

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06723795 on ClinicalTrials.gov ↗ ← All trials in Israel