Actively Recruiting

Age: 18Years - 120Years
All Genders
NCT06410274

Ischaemic Lesions in Acute Intracerebral Haemorrhage

Led by University of Leicester · Updated on 2024-09-19

120

Participants Needed

1

Research Sites

243 weeks

Total Duration

On this page

Sponsors

U

University of Leicester

Lead Sponsor

U

University Hospitals, Leicester

Collaborating Sponsor

AI-Summary

What this Trial Is About

The aim of this observational study is to determine how and why inadequate brain blood flow occurs after bleeding in patients with intracerebral haemorrhage (ICH). Treatment for strokes caused by burst blood vessels involves reducing blood pressure (BP) to stop the bleeding. However, this reduction in BP may affect blood flow, causing blockages in blood vessels within the brain. Fast breathing also affects brain blood flow. Therefore, participants will be asked to undergo a simple brain blood flow assessment using transcranial Doppler (TCD) within 48 hours upon admission to hospital. Patients will then have a follow-up TCD assessment at 4-7 days post-ICH onset, in addition to an MRI scan at \>7 days. This research will help to confirm if blockages after bleeding are caused by reduced blood flow within the brain.

CONDITIONS

Official Title

Ischaemic Lesions in Acute Intracerebral Haemorrhage

Who Can Participate

Age: 18Years - 120Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Clinical diagnosis of haemorrhagic stroke on CT imaging within 48 hours of onset
  • Male or female aged 18 years or older
Not Eligible

You will not qualify if you...

  • MRI imaging contraindicated or patient clinically unstable (Glasgow Coma Scale less than 8, unable to lie supine)
  • Patients requiring anesthesia
  • Age under 18 years
  • Stroke diagnosis more than 48 hours after onset

AI-Screening

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Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

University Hospitals of Leicester NHS Trust

Leicester, United Kingdom, LE1 5WW

Actively Recruiting

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Research Team

J

Jatinder Minhas, SFHEA

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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