Early Multimodal Neuromonitoring For Spontaneous Intracerebral Hemorrhage (ICH)

NCT05501613 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 65

Last updated 2023-02-06

No results posted yet for this study

Summary

The investigators intend to assess the predictive value of early (first 48 hours) multimodal neuromonitoring parameters concerning late survival in critically ill intracerebral hemorrhage (ICH) patients.

Conditions

  • Intracerebral Hemorrhage
  • Critically Ill
  • Intracranial Pressure
  • Cerebral Perfusion Pressure
  • Prognostic

Interventions

DIAGNOSTIC_TEST

Multimodal Neuromonitoring

Invasive Multimodal Neuromonitoring

Sponsors & Collaborators

  • Universidade do Porto

    lead OTHER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-01-31
Primary Completion
2022-10-01
Completion
2023-02-01

Countries

  • Portugal

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 NCT05501613 on ClinicalTrials.gov