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Validation of UK Protocols to Exclude Brain Blood Flow During Normothermic Regional Perfusion (NRP)

NHS Foundation Trust logo

NHS Foundation Trust

Status

Not yet enrolling

Conditions

Cerebral Blood Flow

Treatments

Procedure: CT angiogram

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

This study aims to evaluate both Abdominal Normothermic Regional Perfusion (A-NRP) and Thoracoabdominal-NRP (TA-NRP) techniques, proving that brain blood flow is not resumed during NRP. This will be assessed through the use of two modalities: CT angiogram of the brain and continuous Hb02 readings. The study group hypothesise that such assessment methods will provide evidence to indicate that brain blood flow is not present during NRP and promote trust in the use of such novel techniques in routine practice.

Enrollment

10 estimated patients

Sex

All

Ages

18 to 75 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • DCD donors in Cambridge University Hospital
  • Planned A-NRP
  • Consent for study has been obtained
  • Those who meet the appropriate criteria for DCD donation following WOLST
  • ≥ 18 years of age
  • ≤ 75 years of age

Exclusion criteria

  • DBD organ donors
  • DCD organ donations outside of Cambridge University Hospital
  • DCD donors without planned A-NRP
  • DCD donors whose family have withheld consent for brain blood flow investigations.
  • Patients who do not meet the appropriate criteria for DCD donation following WOLST
  • Patients with injuries that will physically prevent use of the necessary assessment methods

Trial design

10 participants in 2 patient groups

A-NRP
Treatment:
Procedure: CT angiogram
TA-NRP
Treatment:
Procedure: CT angiogram

Trial contacts and locations

0

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Central trial contact

Antonio Rubino; Thomas Howlett

Data sourced from clinicaltrials.gov

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