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Clinical Trials/NCT05771662
NCT05771662
Recruiting
Not Applicable

Multimodal Brain Monitoring as a Prognostic Tool for Intracerebral Hemorrhage - A Prospective Observational Cohort Study.

Universidade do Porto1 site in 1 country25 target enrollmentApril 1, 2021

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Intracerebral Hemorrhage
Sponsor
Universidade do Porto
Enrollment
25
Locations
1
Primary Endpoint
Relation between multimodal brain monitoring parameters and outcome.
Status
Recruiting
Last Updated
3 years ago

Overview

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.

Registry
clinicaltrials.gov
Start Date
April 1, 2021
End Date
September 30, 2023
Last Updated
3 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Spontaneous Intracerebral Hemorrhage
  • ICU admission in the first 24hours
  • Need for intraparenchymal Neuromonitoring
  • Over 18 years old

Exclusion Criteria

  • Tumour, Trauma or known Vascular Lesion
  • Pregnancy

Outcomes

Primary Outcomes

Relation between multimodal brain monitoring parameters and outcome.

Time Frame: 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 Outcomes

  • ICH Neuromonitoring and Short Term Outcome(28 days)
  • ICH Neuromonitoring Pattern.(7 days)

Study Sites (1)

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