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Multimodal Brain Monitoring as a Prognostic Tool for Intracerebral Hemorrhage

NCT ID: NCT05771662

Last Updated: 2023-03-16

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Total Enrollment

25 participants

Study Classification

OBSERVATIONAL

Study Start Date

2021-04-01

Study Completion Date

2023-09-30

Brief Summary

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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.

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Detailed Description

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Conditions

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Intracerebral Hemorrhage

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Eligibility Criteria

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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
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Universidade do Porto

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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Centro Hospitalar São João

Porto, , Portugal

Site Status RECRUITING

Countries

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Portugal

Facility Contacts

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Ana Ferreira, MD

Role: primary

[email protected]
00351917529471 ext. 31917

Other Identifiers

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ICH-NEUROICU

Identifier Type: -

Identifier Source: org_study_id

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