Metabolomics Study on Postoperative Intensive Care Acquired Muscle Weakness

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorTechnical University of Munich

About this trial

In this mono-center pilot trial, surgical patients who are at high risk to be admitted to intensive care will be screened and asked for participation. We are going to take blood and muscle samples at respecified time points to do metabolic, histological and molecular testing.

Aim of the study is to investigate (1) changes of the blood metabolome in patients with ICUAW (intensive care unit acquired weakness) and (2) identify metabolic components who are responsible for ICUAW or can be used as marker for ICUAW.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

invasive mechanically ventilated critically ill patient with expected intensive care unit stay > 3 days

postoperative patient

≥ 18 years old

American Society of Anesthesiology (ASA) classification ≥ III

Disqualifiers

moribund patient

non-curative care (comfort care)

Trial population

mechanically ventilated postoperative high-risk patients who are admitted to intensive care

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

20 Participants
are grouped into 2 trial groups
Group A: Intensive Care Patients
Group B: Operative Control patients

Trial outcomes

Primary outcomes

1

Metabolomics

Blood Metabolome will be isolated from blood samples. All samples will be screened for influence of Intensive Care Unit Acquired Weakness (ICUAW) using mass spectrometry.

Time frame
a median of 14 days

Secondary outcomes

1

Muscle histology

Immunohistochemistry will be done in muscle samples. All samples will be screened for influence of Intensive Care Unit Acquired Weakness (ICUAW) and correlation with blood metabolome changes.

Time frame
a median of 14 days
2

Phosphoproteomics

Phosphoproteomics will be done in muscle samples using mass spectrometry. All samples will be screened for influence of Intensive Care Unit Acquired Weakness (ICUAW) and correlation with blood metabolome changes.

Time frame
a median of 14 days

Other outcomes

1

Identify possible predictors of muscle wasting in the blood metabolome preoperatively

Among the blood metabolome that will be measured, identify metabolites or combinations of metabolites whose high or low concentration(s) preoperatively associate(s) with the amount of muscle loss. These metabolites are candidate biomarkers that could be used to identify individuals at risk of large muscle wasting and may give further insights into the mechanisms of muscle wasting.

Time frame
a median of 14 days
2

Identify possible predictors of muscle wasting in the blood metabolome at ICU admission

Among the blood metabolome that will be measured, identify metabolites or combinations of metabolites whose high or low concentration(s) at ICU admission associate(s) with the amount of muscle loss. These metabolites are candidate biomarkers that could be used to identify individuals at risk of large muscle wasting and may give further insights into the mechanisms of muscle wasting.

Time frame
a median of 14 days

Sponsors and contacts

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Technical University of Munich

Lead sponsor

Medical University of Vienna

Sponsor institution

Helmholtz Zentrum München

Collaborator

Charite University, Berlin, Germany

Collaborator

Medical University of Vienna

Collaborator