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ProAdrenomedullin Assessment of Multi-Organ Failure in COvid-19 Sepsis

ProAdrenomedullin Assessment of Multi-Organ Failure in COvid-19 Sepsis

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04522310
Acronym
PAMOCOS
Enrollment
183
Registered
2020-08-21
Start date
2020-07-07
Completion date
2021-05-29
Last updated
2021-08-05

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

Conditions

Covid19

Brief summary

COVID-19 is a worldwide pandemic. Around 5% of infected patients are admitted in ICU, mainly for respiratory failure. Outcome of these patients is linked to other organ failures. Optimal therapies are not defined so far. The sponsor want to assess the role of MR-ProADM as prognostic biomarker, and the impact of treatments (including supportive treatments) on MOF occurrence and outcome.

Interventions

OTHERMR-Pro-ADM

Dosage of MR-pro-ADM

Sponsors

Centre Hospitalier de Lens
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

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

Inclusion criteria

* Any adult patient admitted in the ICU with COVID-19 pneumonia

Exclusion criteria

* Pregnancy * Legal reasons (patients under guardianship, curatorship) * Patient's refusal

Design outcomes

Primary

MeasureTime frameDescription
Association or correlation between MR-ProADM at day 1 and day 3 and the onset of visceral failures extra respiratory in reanimation.comparison to day 1 and day 3Association or correlation between MR-ProADM at day 1 and day 3 and the onset of visceral failures extra respiratory in reanimation.
mortality at day 28 and day 90.admission until day 90mortality at day 28 and day 90.

Secondary

MeasureTime frameDescription
Association between MR-ProADM and mortality at day 28.admission until day 28Association between MR-ProADM and mortality at day 28.
Association or correlation between patient factor or treatment, and the onset or aggravation of visceral failures (day 3 and day 10), evolution until day 28.admission until day 28Association or correlation between patient factor or treatment, and the onset or aggravation of visceral failures (day 3 and day 10), evolution until day 28.

Countries

France

Outcome results

None listed

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