MedPath

Multimodal Brain Monitoring as a Prognostic Tool for Intracerebral Hemorrhage

Recruiting
Conditions
Intracerebral Hemorrhage
Registration Number
NCT05771662
Lead Sponsor
Universidade do Porto
Brief Summary

To verify if there is an association between advanced multimodal brain monitoring parameters in the first 48h and fist 7 days of admission with intrahospital and six-months functional outcome, even when controlled to other factors that may influence the outcome. Secondary Goals: To describe multimodal neuromonitoring parameters variation in the first seven days of ICH and identify any trends.

Detailed Description

Not available

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
25
Inclusion Criteria
  • Spontaneous Intracerebral Hemorrhage
  • ICU admission in the first 24hours
  • Need for intraparenchymal Neuromonitoring
  • Over 18 years old
Read More
Exclusion Criteria
  • Tumour, Trauma or known Vascular Lesion
  • Pregnancy
Read More

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Relation between multimodal brain monitoring parameters and outcome.6 months

Association between advanced multimodal brain monitoring parameters of the first 48h of admission and six months functional outcome (Glasgow Outcome Score Extended)

Secondary Outcome Measures
NameTimeMethod
ICH Neuromonitoring and Short Term Outcome28 days

Association between advanced multimodal brain monitoring parameters and 28 days functional outcome (Glasgow Outcome Score Extended)

ICH Neuromonitoring Pattern.7 days

Describe multimodal neuromonitoring parameters variation in the first seven days of ICH and identify trends.

Trial Locations

Locations (1)

Centro Hospitalar São João

🇵🇹

Porto, Portugal

© Copyright 2025. All Rights Reserved by MedPath