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Prevalence of inflammation in patients with cardiovascular disease and heart failure.

POSEIDON – Prevalence of systemic inflammation in patients with atherosclerotic cardiovascular disease and heart failure

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2024/05/067153
Enrollment
21504
Registered
2024-05-10
Start date
Unknown
Completion date
Unknown
Last updated
2024-05-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: I251- Atherosclerotic heart disease of native coronary artery

Interventions

Intervention1: NIL: NIL Control Intervention1: NIL: NIL

Sponsors

Novo Nordisk AS
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Informed consent obtained before any study-related activities. Study-related activities are any procedures that are carried out as part of the study. 2. Age 18 years or above at the time of signing the informed consent. 3. Presence of ASCVD and/or HF. 4. Presence of serum creatinine in the medical chart within 24 months prior to signing of informed consent (for ASCVD patients only).

Exclusion criteria

Exclusion criteria: 1. Previous participation in this study. Participation is defined as having given informed consent in this study. 2. Current participation (i.e., signed informed consent) in any other interventional clinical study. 3. Any hospitalization or unplanned visit within the last 60 days (including exacerbation of chronic disease with hospitalization). 4. Clinical evidence, or suspicion of, active infection within the last 60 days. 5. Mental incapacity, unwillingness, or language barriers precluding adequate understanding or cooperation

Design outcomes

Primary

MeasureTime frame
To estimate the prevalence of systemic inflammation (defined as hsCRP =2 mg/L) in pre-defined cohorts of patients with ASCVD and/or HF, and subgroups hereof.Timepoint: Primary objective will be assessed during subject visit date and there is only one subject visit in this study.

Secondary

MeasureTime frame
• To examine IL-6 stratified by the presence of systemic inflammation (defined as hsCRP =2 mg/L) in pre-defined cohorts of patients with ASCVD and/or HF, & subgroups hereof. • To examine NT-proBNP stratified by the presence of systemic inflammation (defined as hsCRP =2 mg/L) in pre-defined cohorts of patients with HF, & subgroups hereof. Timepoint: Secondary objective will be assessed during subject visit date & there is only one subject visit in this study.

Countries

Argentina, Australia, Brazil, Canada, China, Czech Republic, Denmark, France, Germany, Hungary, India, Italy, Japan, Norway, Poland, Republic of Korea, Sweden, United Kingdom, United States of America

Contacts

Public ContactJinu Jose

IQVIA RDS (India) Private Limited

jinu.jose@iqvia.com9886203019

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026