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Clinical Trials in Germany / NCT07053631
Recruiting Not applicable

Investigation of a New Window Into Intracranial Pressure: Venous Occlusion Pressure of the Isolated Periorbital Vein

NCT07053631 · tracked via the Priya Life Science Germany tracker
Phase
Not applicable
Started
2025-04-07
Last updated
2025-07-08

Condition(s) studied

Indication for CSF Dynamic TestingIndication for CSF Infusion Test

Investigational drug(s) / intervention(s)

venous occlusion pressure Measurement

venous occlusion pressure Measurement: non-invasive venous occlusion pressure of a targeted periorbital vein is measured in parallel to clinical standard CSF dyanmic testing including standard CSF infusiontest

Study summary

Elevated intracranial pressure (ICP) occurs when pressure inside the skull rises above normal levels, potentially leading to brain damage or herniation. Monitoring ICP is critical for managing conditions like brain tumors, traumatic brain injury, and stroke. Current ICP monitoring methods are invasive and carry risks, including infection and brain damage. For less severe cases, lumbar puncture is a safer, less invasive alternative. This study explores the potential of a non-invasive method, using venous pressure near the eye, to estimate ICP. The goal is to assess whether the results from this non-invasive approach are similar to the invasive lumbar CSF pressure measurements.

Eligibility

Sex
ALL
Min age
18 Years
Max age
95 Years
Healthy volunteers
No
Inclusion Criteria: * Medical indication to perform routine craniospinal CSF dynamic testing according to standard operative procedures * Aged 18-95 * Willing and able to provide valid signed informed consent Exclusion Criteria: * Patients with any known ongoing, or history of, abnormal CSF communication * Patients with any kind of prior intervention for CSF diversion * Patients with acute brain damage within the preceding 6 months * Patients with transdural surgery within the preceding 6 months * Head wounds or hematoma that could hinder access to measurement site * Any known pathological condition linked to the orbital socket influencing venous outflow

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Klinik für Neurochirurgie, Universitätsklinikum Freiburg Freiburg im Breisgau Germany Recruiting

More University of Freiburg trials in Germany

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07053631 on ClinicalTrials.gov ↗ ← All trials in Germany