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UNKNOWNNA

Electrocorticographic Monitoring of Brain Retraction Injury (EMBRI)

Sponsor: University College, London

NCT ID: NCT06409806

View on ClinicalTrials.gov ↗

At a glance

What the study gets you
Access to the study treatment being tested
Type of study
Interventional (receives a drug or procedure)
Time in hospital
In-person visits at study sites — visit count not specified by the sponsor
Drug or intervention
ECOG Array (other)
How long the study runs
Study runs about 43 months (dates as stated)
About the drug or intervention
ECOG Array — other: The patient will undergo their intracranial neurosurgical procedure as planned, using conventional brain retractors and neurosurgical equipment.
Patient visit burden
Not specified by the sponsor
Type of study
Testing a treatment
Ages
16 Years and over
Who
All
Number of participants
6
Started
2022-08-01
Last checked
2024-09

Plain English Summary

What is this study?

  • • Testing a new treatment for brain injury
  • • NA - 6 participants
  • • A single centre IDEAL Stage 1 feasibility study using novel electrophysiological recording techniques in adult participants undergoing neurosurgery

Who can take part?

  • • Ages 16 Years and over
  • • Diagnosed with brain injury

Where?

  • • London - National Hospital Neurology and Neurosurgery

This is a simplified summary. Always discuss with your doctor before making any decisions.

About This Trial

A single centre IDEAL Stage 1 feasibility study using novel electrophysiological recording techniques in adult participants undergoing neurosurgery. This is a first in human study, building upon previous preclinical mice experiments. Participants will undergo their planned neurosurgical procedure as normal. In addition to their standard treatment neurophysiological monitoring including an electrocorticography electrode placed on the brain deep to the retractor will be used to monitor for signs of brain retraction injury.

Brain InjuryNeurosurgeryBrain Ischemia

How this trial compares with your answers

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What we know so far

Condition· Matched your search
Age· Tell us your age for better matching
Gender· Tell us your sex for better matching

Still need:

  • • Tell us your age for better matching
  • • Tell us your sex for better matching

Preliminary match based on your answers. Full eligibility requires on-site assessment including medical history, physical exam, and lab tests. This does not guarantee enrolment.

Eligibility at a Glance

Key info

  • Age: 16 Years and over
  • Who can join: All genders

What the study is looking for

  • ✓Patients aged 16 or older undergoing intracranial surgery where it is anticipated fixed brain retraction will be used.

Who cannot take part

  • ✗Patients without capacity to give consent at time of recruitment
See the full criteria
Inclusion Criteria: * Patients aged 16 or older undergoing intracranial surgery where it is anticipated fixed brain retraction will be used. Exclusion Criteria: * Patients without capacity to give consent at time of recruitment

Where Is This Study? (1 UK site)

National Hospital Neurology and Neurosurgery

London WC1N 3BG, United Kingdom

Recruiting
Site contact (verified)

How to Get in Touch

Siddharth Sinha

Sponsor contact

CONTACT

004420 3456 7890 siddharth.sinha@ucl.ac.uk
Data sourced from ClinicalTrials.gov · Last verified: 2024-09