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OpenTrials
Completed

NCT Number: NCT02326571

Multimodal Monitoring in Patients With Spontaneous Intracerebral Hemorrhage

Spontaneous intracerebral bleeding also known as spontaneous intracerebral hemorrhage (sICH) constitute 10-15 % of all apoplexies. The Prognosis is considerably worse than it is for the larger population of patients suffering from cerebral thrombosis. Development of brain edema seemingly contributes to the disadvantageous prognosis. However, the mechanisms behind is only understood fragmentarily.

By using multimodal neuro monitoring, the investigators seek to investigate electrophysiological and metabolic processes, which seem to accompany the formation of edema and clinical deterioration in patients suffering from sICH.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Rigshospitalet, NICU

Copenhagen, 2100, Denmark

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Diagnosis: spontaneous intracerebral hemorrhage verified by CT
  • Clinical indication for craniotomy or craniectomy
  • Admitted to the hospital within 24 hours from assumed ictus
  • Age over 18 years

Exclusion criteria

  • Pregnancy

Treatment and study plan

Primary outcomes

  1. Secondary brain injury

    Time frame: 10 days

    Assessed by GCS, CAM-ICU, mRS, Imaging, EEG background activity.

Sponsors and collaborators

Lead sponsor

Christian Kærsmose Friberg

Other

Registry information

Important dates

Study start
2014
Primary completion
2016
Study completion
2016
First posted
Dec 29, 2014
Registry last updated
Apr 11, 2017

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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