NCT03221959

Non-invasive Absolute Intracranial Pressure Measurement in Patients With Malignant Middle Cerebral Artery Infarction for Determination of Timing to Descompressive Craniectomy.

Non-invasive Absolute Intracranial Pressure Measurement in Patients With Malignant Middle Cerebral Artery Infarction for Determination of Timing to Decompressive Craniectomy
Kienzler Jenny·ClinicalTrials.gov·device·Device trial
View on ClinicalTrials.gov
Study focus
Drug/Device/Intervention
Medical Device Vittamed 205
Study type
Observational
Intervention type
device
Sponsor & location
Primary sponsor
Kienzler Jenny
Funder
Kantonsspital Aarau
Timeline & enrollment
Phase
N/A
Start date
Jan 01, 2018
End date
Dec 01, 2020
Enrollment
48 participants
Primary outcome

non-invasive ICP) measurement im mmHg

Summary

This is a single centre, observational study with a medical device which has Conformité
 Européenne (CE) marking. The aim of the study is to demonstrate that patients with malignant
 middle cerebral artery infarction (M-MCA) show an increased intra-cranial pressure (ICP)
 compared to neurological patients without M-MCA infarction or other space-occupying
 indications.

ICD-10 classifications
Benign intracranial hypertensionIntracranial injuryIntracranial injury, unspecifiedOther intracranial injuriesIntracranial hypotension following ventricular shunting
Data source
Registry
ClinicalTrials.gov
Trial ID
NCT03221959
Type
Device Trial
About this record

Access comprehensive clinical trial information for NCT03221959 through Pure Global AI's free database. This phase not specified trial is sponsored by Kienzler Jenny and is currently status unknown. The study focuses on Intracranial Pressure Increase. Target enrollment is 48 participants.

This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.