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A single-center comparative study of ICP monitoring by external ventricular drainage hydraulic coupling and by brain parenchymal monitoring

Establish a standardized technical system for monitoring ICP through external ventricular drainage connected to an arterial pressure converter

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500109992
Enrollment
Unknown
Registered
2025-09-28
Start date
2019-07-10
Completion date
Unknown
Last updated
2025-10-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Neurological diseases

Interventions

EVD group:NA
ICP group:NA

Sponsors

Qilu Hospital of Shandong University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Neurocritical patients with GCS = 8 points, including those with craniocerebral trauma (GCS = 8 points) and those with cerebral hemorrhage (GCS = 8 points). 2. The patient needs to undergo ICP monitoring (including both extracorporeal ventricular drainage type ICP monitoring and brain parenchymal type ICP monitoring). 3. The patient's age ranges from 18 to 70 years old.

Exclusion criteria

Exclusion criteria: Those who have interrupted ICP monitoring; When a patient agrees to participate in the study and voluntarily requests to withdraw from the experimental study at any time, the patient's clinical data and specimens will no longer be included in this study.

Design outcomes

Primary

MeasureTime frame
ICP value;—

Secondary

MeasureTime frame
Degree of compliance with ICP;Analysis of ICP waveform;—

Countries

China

Contacts

Public ContactQibing Huang

Qilu Hospital of Shandong University

hqibing@outlook.com+86 185 6008 3135

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026