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Status unknownNCT02885675Updated Aug 31, 2016

An Observational Study of the Correlation Between miRNA in Peripheral Blood and Prognosis in Patients With ARDS

An observational study in ARDS, sponsored by Southeast University, China. Status unknown at 1 site in China. Open to participants aged 18 Years to 85 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2016-08-31.

Sponsored by Southeast University, China · Observational

The sponsor has not verified this record recently (last verified Aug 2016), so the status shown — last known as Recruiting — may be out of date.
Study type
Observational
Model
Case-control
Time perspective
Prospective
Enrollment
80
Ages
18 Years to 85 Years
Sex
All
01

Study summary

To evaluate the correlation between the value of miRNA related to ARDS and vascular endothelial cell and ARDS severity, vascular endothelial cell damaging degree,mortality in patients with ARDS.

Read the detailed description

After consulting literature, we obtain 14 miRNAs related to ARDS and vascular endothelial cell(ARDS-VEC-miRNAs) and 2 biomarkers of scathing vascular endothelial.The ARDS-VEC-miRNAs include miR-15a-5p,miR-16-5p,miR-21-5p,miR-24-3p,miR-26a-5p,miR-27a-3p,miR-27b-3p,miR-126-3p,miR-150-5p,miR-146a-5p,miR-155-5p,miR-221-3p,miR-223-3p,miR-320a.The biomarkers of scathing vascular endothelial include vascular cell adhesion molecule-1(VCAM-1),von Willebrand factor(vWF).20 healthy controls and 60 patients diagnose as ARDS in ICU were included in this study.we blood every participants within 24 hours after enrollment and obtain the plasma.Then, we detecte ARDS-VEC-miRNAs,VCAM-1,vWF levels in plasma by real-time quantitative PCR,record the severity of the illness and survival status within 28 days of every patients.Finally,we evaluate the correlation between the value of miRNA related to ARDS and vascular endothelial cell and ARDS severity, vascular endothelial cell damaging degree,mortality in patients with ARDS.

02

Conditions studied

  • ARDS
03

In context

Lead sponsor

Southeast University, China is the lead sponsor of 164 studies on the registry; 44 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 85 Years
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Probability sample

Study population

20 healthy controls and 60 patients diagnose as ARDS in ICU were included in this study.

Eligibility criteria

Inclusion Criteria:(1)Admitted to ICU, ARDS patients(Berlin criteria), (2)Patients diagnosed ARDS within 24 hours, (3)Patients age between 18 years old and 85 years.

Exclusion Criteria:1)Pregnant women, 2)Patients with malignant tumor, 3)Immunosuppression or immunocompromised patients.

05

Study design

Observational model
Case-control
Time perspective
Prospective
Enrollment
80 participants (estimated)
Patient registry
No

Groups and cohorts

  • ARDS

    Other: blood sampling

  • Healthy control

    Other: blood sampling

Interventions

  • Otherblood sampling

    sample no more than 3ml

06

What researchers measure

Primary outcomes

  1. mortality

    Time frame: 28-day

07

Study locations

1 of 1 sites recruiting
  • Zhong-Da hospital
    Nanjing, Jiangsu 210009, China
    • Huang Yingzi, doctor · Contact · +8613951693278
    • Zheng Yi, postgraduate · Sub investigator
    Recruiting
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 31, 2016, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT02885675
Lead sponsor
Southeast University, China
Responsible party
Jianfeng Xie (Zhongda Hospital, Southeast University, China) — Principal investigator
First posted
Aug 31, 2016
Start date
Mar 2016
Primary completion
Feb 2017 (estimated)
Completion
Feb 2017 (estimated)
Last update
Aug 31, 2016

Study contacts

Hunag Yingzi, doctor
Contact
yz_huang@126.com
+8613951693278
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Aug 2016. You cannot join it, but the record below documents what was studied.

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