MicroRNA Diagnostics in Subarachnoid Hemorrhage 2

NCT02320539 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 70

Last updated 2015-05-27

No results posted yet for this study

Summary

The purpose of this study is to validate results from a related trial (NCT01791257) and to compare the profile of microRNA in blood from patients suffering subarachnoid hemorrhage with and without systemic complications.

Conditions

  • Subarachnoid Hemorrhage
  • Delayed Cerebral Ischemia
  • Acute Lung Injury
  • Cardiac Dysfunction
  • Systemic Inflammatory Response Syndrome

Sponsors & Collaborators

  • Rigshospitalet, Denmark

    lead OTHER

Principal Investigators

  • Kirsten Møller, Prof · Neurointensive Care Unit, The Neuroscience Center, Rigshospitalet

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2014-11-30
Primary Completion
2015-05-31
Completion
2015-05-31

Countries

  • Denmark

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02320539 on ClinicalTrials.gov