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临床试验/NCT07466524
NCT07466524已完成不适用

suPAR ≥6 ng/mL for Predicting Severe Respiratory Failure in U.S. Adults Hospitalized With COVID 19 (suPAR US The Michigan Cohort Heterogeneity Study)

ViroGates A/S1 个研究点 分布在 1 个国家目标入组 367 人开始时间: 2020年2月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
367
试验地点
1
主要终点
Severe respiratory failure (SRF) within 30 days

研究概览

简要总结

This is a retrospective, non interventional cohort study using stored plasma samples from appoximately 300 adults hospitalized with confirmed COVID 19. Baseline suPAR measured using the suPARnostic TurbiLatex assay on the Roche cobas c501.

详细描述

The Michigan Medicine COVID-19 Cohort (M2C2) is the largest sub-cohort of the International Study on Inflammation in COVID-19 (ISIC). The M2C2 comprises consecutive, systematically enrolled adults (≥18 years) with confirmed SARS-CoV-2 infection hospitalized specifically for COVID-19 at the University of Michigan from 1 February 2020 to 1 June 2021. Adult patients hospitalized in participating U.S. hospitals with confirmed COVID 19 infection during the study period, who had baseline suPAR measured using the suPARnostic TurbiLatex assay on Roche cobas c501 on plasma samples obtained within 48 hours of admission. The cohort reflects real world U.S. data and includes racially and ethnically diverse populations with typical U.S. burdens of obesity, diabetes, and chronic kidney disease.

SAMPLE SIZE JUSTIFICATION - Since we have a fixed 6 ng/mL threshold and are only validating (not discovering), the analysis is just a 2×2 table.

True sensitivity 94% (matching SPARCOL): N=136 is enough True sensitivity 90% (conservative): N=237 is enough True sensitivity 88% (worst case): N=440 needed SPARCOL showed 93.9%, so N=300 covers you even if U.S. sensitivity drops to ~88% - a generous safety margin.

STATED LIMITATIONS

  • N=300 does not support fully adjusted multivariable logistic regression
  • Hispanic and Asian subgroups are too small for standalone powered analyses. These subgroups are reported descriptively.
  • Formal non-inferiority testing of sensitivity (U.S. vs. SPARCOL) would require a larger sample. The comparison is performed descriptively, with the acceptance criterion applied to the U.S. data independently (lower 95% CI > 80%).

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Retrospective

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Inclusion Criteria
  • Age ≥18 years at hospital admission.
  • Confirmed SARS CoV 2 infection documented in the EHR (positive RT PCR or antigen test from a respiratory specimen).
  • suPAR level measured from EDTA plasma using the suPARnostic TurbiLatex assay on a Roche cobas c501 analyzer on samples taken within 24 hours of Emergency Department presentation or hospital admission.
  • Available 30 day follow up data from the date of admission (30 day vital status and SRF status ascertainable).

排除标准

  • Already intubated and/or receiving invasive mechanical ventilation at the time of suPAR sample collection.
  • Documented "Do Not Intubate" order or determination that the patient was not a candidate for mechanical ventilation at admission.
  • suPAR measured by a method other than the suPARnostic TurbiLatex assay on Roche cobas c501 (e.g., ELISA, other platforms).
  • Incomplete primary endpoint data (SRF status cannot be determined within 30 days).
  • Patients with confirmed SARS CoV 2 infection who were not primarily admitted for COVID 19 (incidental positive test in a non COVID admission).

研究组 & 干预措施

Michigan Medicine Cohort Study

The Michigan Medicine Cohort (M2C2) is part of the International Study of Inflammation in COVID-19 (ISIC), ClinicalTrials.gov ID NCT04818866

干预措施: suPARnostic® TurbiLatex Assay on Roche cobas c501 (Diagnostic Test)

结局指标

主要结局

Severe respiratory failure (SRF) within 30 days

时间窗: Statistical analysis will be carried out in March 2026

Development of severe respiratory failure requiring endotracheal intubation and initiation of invasive mechanical ventilation within 30 days of hospital admission. SRF is ascertained from EHR procedure codes and clinical documentation. Performance metrics (sensitivity, specificity, PPV, NPV, AUC) at the suPAR ≥6 ng/mL threshold will be calculated.

次要结局

  • Secondary outcomes (optional)(March 2026)
  • Subgroup analysis(March 2026)
  • Composite endpoint(March 2026)

研究者

发起方
ViroGates A/S
申办方类型
Industry
责任方
Sponsor

研究点 (1)

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