ClinicalTrials.Veeva

Menu

Metabolomics and Microbiomics in Cardiovascular Diseases (MEMORIA)

U

Universitätsmedizin Mannheim

Status

Unknown

Conditions

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

Treatments

Other: Blood draw

Study type

Observational

Funder types

Other

Identifiers

NCT04146701
2019-1093N-MA

Details and patient eligibility

About

"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.

Full 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.

Enrollment

750 estimated patients

Sex

All

Ages

18 to 100 years old

Volunteers

Accepts Healthy Volunteers

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

Trial design

750 participants in 7 patient groups

Acute heart failure
Description:
All consecutive patients admitted with acute heart failure to University Medical Center Mannheim. One venous blood withdraw will be performed. Demographic and clinical data will be documented.
Treatment:
Other: Blood draw
STEMI
Description:
All consecutive patients admitted with STEMI to University Medical Center Mannheim. One venous blood withdraw will be performed. Demographic and clinical data will be documented.
Treatment:
Other: Blood draw
NSTEMI
Description:
All consecutive patients admitted with NSTEMI to University Medical Center Mannheim. One venous blood withdraw will be performed. Demographic and clinical data will be documented.
Treatment:
Other: Blood draw
Ischemic cardiomyopathy
Description:
All consecutive patients with an implantable cardioverter defibrillator (ICD) due to ischemic cardiomyopathy and LVEF \<35% presenting for ICD check-up to University Medical Center Mannheim. One venous blood withdraw will be performed. Demographic and clinical data will be documented.
Treatment:
Other: Blood draw
Non-ischemic cardiomyopathy
Description:
All consecutive patients with an implantable cardioverter defibrillator (ICD) due to non-ischemic cardiomyopathy and LVEF \<35% presenting for ICD check-up to University Medical Center Mannheim. One venous blood withdraw will be performed. Demographic and clinical data will be documented.
Treatment:
Other: Blood draw
Sepsis
Description:
All consecutive patients admitted with sepsis or septic shock to University Medical Center Mannheim. One venous blood withdraw will be performed. Demographic and clinical data will be documented.
Treatment:
Other: Blood draw
Healthy controls
Description:
Clinically inapparent group as controls. One venous blood withdraw will be performed. Demographic and clinical data will be documented.
Treatment:
Other: Blood draw

Trial contacts and locations

1

Loading...

Central trial contact

Ibrahim Akin, Prof. Dr.; Michael Behnes, PD Dr.

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2025 Veeva Systems