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Retrospective Study of Intracerebral Hemorrhage Patients in Hospital Parc Taulí

A

Autonomous University of Barcelona

Status

Completed

Conditions

Intracerebral Hemorrhage

Treatments

Other: No intervention

Study type

Observational

Funder types

Other

Identifiers

NCT04877405
UHA-2021-1

Details and patient eligibility

About

This is a retrospective observational study to investigate the clinical, analytical and neuroimaging data generated during routine clinical management of intracerebral hemorrhage. The study will review the data from about 500 patients attended during the last ten years in the Neurology Department of Hospital Parc Taulí de Sabadell.

The aim is to measure the size of the lesion in neuroimage (TC and MRI), the edema, the alterations in diffusion weighted images and to correlate this data with clinical parameters and analytical measurements. With this approach investigators plan to investigate the incidence of hematoma growth, the role of perilesional edema and diffusion changes, and the relation between neuroimaging findings and clinical outcome. The study also try to establish significant correlations between clinical and analytical data, the clinical outcome and and the magnitude of changes in neuroimaging.

Enrollment

137 patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients who have been attended at the Hospital Parc Taulí for the last 10 years after presenting an intraparenchymal hemorrhage.
  • The patients have had to undergo a computed tomography at the admission and a cranial magnetic resonance during the hospitalization in the time course specified in point in the protocol
  • The patients must present in their clinical story the analytical determinations detailed in the protocol.

Exclusion criteria

  • Intracerebral hemorrhage secondary to head trauma
  • Intracerebral hemorrhage secondary to neoplasm

Trial design

137 participants in 1 patient group

Intracerebral hemorraghe
Description:
Patients that suffered an intracerebral hemorraghe and that have been subjected to CT and MRI scans
Treatment:
Other: No intervention

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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