MicroRNA Diagnostics in Subarachnoid Hemorrhage

NCT01791257 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 50

Last updated 2014-04-08

No results posted yet for this study

Summary

The purpose of this study is to compare the profile of microRNA in cerebrospinal fluid from patients suffering subarachnoid hemorrhage with and without delayed cerebral ischemia.

Conditions

  • Subarachnoid Hemorrhage

Sponsors & Collaborators

  • Bispebjerg Hospital

    collaborator OTHER
  • Rigshospitalet, Denmark

    lead OTHER

Principal Investigators

  • Søren B Larsen, MD · Rigshopsitalet, Denmark

  • Kirsten Møller, DMSci · Rigshospitalet, Denmark

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2013-02-28
Primary Completion
2014-01-31
Completion
2014-01-31

Countries

  • Denmark

Study Locations

More Related Trials

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 NCT01791257 on ClinicalTrials.gov