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Is Bio-adrenomedullin (Bio-ADM) a Prognostic Factor in Patients With COVID-19 Treated in the ICU?

Is Bio-adrenomedullin (Bio-ADM) a Prognostic Factor in Patients With COVID-19 Treated in the ICU?

Status
Terminated
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04813939
Enrollment
32
Registered
2021-03-24
Start date
2021-03-22
Completion date
2022-01-31
Last updated
2022-05-16

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

Conditions

Covid19

Keywords

bio-adrenomedullin, point of care, sepsis

Brief summary

This is prospective, observational study using point of care test to determine bio-ADM whole blood concentrations and its predictive value in patients with COVID-19 treated in the ICU.

Detailed description

About 5% of all patients infected with the SARS-CoV-2 virus require treatment in the ICU. The main reason for admission to the ICU is acute hypoxemic respiratory failure, which in most cases is associated with the need for mechanical ventilation. The progression of lung damage affects not only alveoli but also endothelium of the pulmonary vessels. Occurring endotheliopathy is caused by direct infection with SARS-CoV-2 virus and activation of the immune system leading to an increased inflammatory reaction. Damage to the endothelium barrier with concomitant cytokine storm lead to activation of the coagulation system and formation of microthrombotic events in the vascular bed, resulting in thromboembolic complications and development of multiorgan failure. The reflection of the above pathophysiological phenomena in laboratory tests is a significant increase in the concentration of D-dimers. At present, no specific markers of endotheliopathy in patients with SARS-CoV-2 are known. Adrenomedullin (ADM) is a peptide hormone that plays a key role in regulating the function of the endothelium, by modulating its integrity and permeability, it also has an effect on the vascular muscle, leading to vasodilation. Recently, the role of ADM has been intensively studied, including in sepsis. Several studies have confirmed an association between elevated ADM levels and poor prognosis in sepsis and septic shock. In these studies, measurements of various adrenomedullin precursors and free, biologically active adrenomedullin (bio-adrenomedullin, bio-ADM) were performed. The role of bio-ADM in the course of COVID -19 remains unclear. The aim of the study is to determine the baseline concentration of bio-ADM and to determine the dynamic of the concentration changes in three measurements in patients with COVID-19 during ICU treatment. Additional measurement of bio-ADM will be performed as standard monitoring in patients suspected of septic complications of the course of COVID-19.

Interventions

DEVICEIB10 sphingotest® bio-ADM® apparatus (Sphingotec GmbH, Hennigsdorf, Germany)

Point of care assessment of bio-adrenomedullin concentration will be performed using the IB10 sphingotest® bio-ADM® apparatus (Sphingotec GmbH, Hennigsdorf, Germany) on the 1,3,5-day ICU stay in COVID-19 patients. The method used is a double monoclonal sandwich immunoassay to measure the concentration of C-terminal amidated, biologically active adrenomedullin (bio-ADM) in whole blood. Additional measurement of bio-ADM will be performed as standard monitoring in patients suspected of septic complications of the course of COVID-19.

Sponsors

Medical University of Warsaw
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* age ≥ 18 years * polymerase chain reaction (PCR) confirmed COVID-19 * severe stage of pneumonia caused by SARS-CoV-2 requiring oxygen therapy * informed consent to participate in the study

Exclusion criteria

* qualification to palliative care * life expectancy \< 48 h * mechanical ventilation at the beginning of the hospitalization * transfer from other ICU * pregnancy

Design outcomes

Primary

MeasureTime frameDescription
Mortality28-days28-day mortality will be assessed

Secondary

MeasureTime frameDescription
Sequential Organ Failure Assessment (SOFA) Score and its changes over time28-daysOccurrence of multiorgan failure expressed in SOFA scores
Need for catecholamines28-daysNeed for catecholamines (drug, highest/lowest dose, duration)
Need for renal replacement therapy28-daysNeed for renal replacement therapy (duration)
Need for mechanical ventilation28-daysNeed for mechanical ventilation (duration)
Changes of partial pressure of oxygen in arterial blood (PaO2) / fraction of inspired oxygen (FiO2) during treatment in ICU28-daysPaO2/FiO2
Changes in blood lactate levels28-daysChanges in blood lactate levels (in mg/dl)
Changes C reactive protein (CRP)28-daysChanges CRP (in mg/l)
Changes in procalcitonin levels28-daysChanges in procalcitonin levels (in ng/ml)
Changes in creatinine levels28-daysChanges in creatinine levels (in mg/dl)
Changes in D-dimer28-daysChanges in D-dimer (in ng/ml)

Other

MeasureTime frameDescription
Sepsis complicating the course of COVID-19 during ICU treatment28-daysOccurrence of sepsis complicating the course of COVID-19 during ICU treatment

Countries

Poland

Outcome results

None listed

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