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Investigating CBF and ICP Using DCS

NCT06039098 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 17

Last updated 2024-02-20

No results posted yet for this study

Summary

We aim to acquire data using DCS on patients who are undergoing invasive ICP and ABP monitoring on ITU as part of their normal treatment.

Data will then be correlated to derive various parameters including CBF and BFI.

All interventions are entirely non-invasive.

Conditions

Interventions

DEVICE

DCS

DCS monitoring of brain

Sponsors & Collaborators

  • Barts & The London NHS Trust

    collaborator OTHER

  • Queen Mary University of London

    lead OTHER

Eligibility

Min Age
16 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-01-05
Primary Completion
2023-08-20
Completion
2023-08-20

Countries

  • United Kingdom

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06039098 on ClinicalTrials.gov