Skip to content

Metabolomics and Microbiomics in Cardiovascular Diseases

Metabolomics and Microbiomics in Cardiovascular Diseases

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04146701
Acronym
MEMORIA
Enrollment
750
Registered
2019-10-31
Start date
2019-02-01
Completion date
2022-12-31
Last updated
2021-02-16

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

Conditions

Acute Heart Failure, Cardiomyopathies, Dilated Cardiomyopathy, Ischemic Cardiomyopathy, Myocardial Infarction, Acute, NSTEMI - Non-ST Segment Elevation MI, Sepsis, STEMI - ST Elevation Myocardial Infarction

Brief summary

MEtabolomics and MicrObiomics in caRdIovAscular diseases Mannheim (MEMORIAM) is a single-center, prospective and observational study investigating to identify disease-specific metabolic, respectively microbiomic, patterns of patients with high-risk cardiovascular diseases. High-risk cardiovascular diseases comprise patients suffering from acute heart failure (AHF), ST-segment elevation myocardial infarction (STEMI), non-ST-segment elevation myocardial infarction (NSTEMI), sepsis, septic shock, ischemic and non-ischemic cardiomyopathy.

Detailed description

Scientific evidence about the metabolomic and microbiomic changes in high-risk cardiovascular patients is still lacking. The acute, critical or progressive disease status predestinies to relevant changes in cardiovascular metobolism. High-risk patients in the present trial comprise those with acute heart failure, myocardial infarction (STEMI and NSTEMI), sepsis, septic shock, ischemic and non-ischemic cardiomyopathy with severely reduced left ventricular ejection fraction (LVEF \<35%). Therfore this study investigates to identify disease-specific patterns of metabolic and microbiomic changes. These patterns may help to understand pathophysiology at the metabolic stages and find out those patients being at highest risk of adverse future outcome.

Interventions

OTHERBlood draw

venous blood withdraw (ca. 40ml)

Sponsors

Universitätsmedizin Mannheim
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 100 Years
Healthy volunteers
Yes

Inclusion criteria

* above mentioned diseases, diagnosis according to respective guideline * written informed consent

Exclusion criteria

* under 18 years * cancer * rheumatic diseases * infections (except septic group) * higher grade heart valve diseases

Design outcomes

Primary

MeasureTime frameDescription
Disease-specific metabolic/microbiomic biomarker patterns.Within 24h after disease onsetExpression of disease-specific metabolic/microbiomic biomarker patterns at the time of acute disease presentation

Secondary

MeasureTime frameDescription
All-cause and cardiovascular mortality.12 months after inclusionAll-cause and cardiovascular mortality, at 6 months and 12 months
Cardiac rehospitalization.12 months after inclusionCardiac rehospitalization, at 6 months and 12 months.

Countries

Germany

Contacts

Primary ContactMichael Behnes, PD Dr.
michael.behnes@umm.de0049 621 383 6239
Backup ContactIbrahim Akin, Prof. Dr.
ibrahim.akin@umm.de0049 621 383 5229

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026