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Recurrent Nerve Monitoring During Aortic Arch Repair — PREMAR  

Recurrent Laryngeal Nerve Injuries Clinical Trial

Official title:
Pilot Study of Recurrent Laryngeal Nerve Monitoring During Neonatal Aortic Arch Repair

Clinical Trial Summary

Almost half of newborns undergoing surgery to repair narrowing or interruption of the aortic arch will suffer injury to the recurrent laryngeal nerve. This causes a weak voice and can lead to problems with feeding including aspiration of milk feed after the surgery. As these children can have a vulnerable circulation, aspiration events can reduce survival and poor weight gain has been shown to correlate with poorer outcomes after surgery. In other types of surgery in the neck, monitors can be used to alert the surgeon to when injury is occurring to the recurrent nerve. To date, this type of monitoring has not been possible in newborns. This study aims to investigate if this type of monitoring is feasible in newborns undergoing aortic arch repair, to prevent recurrent nerve injury.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

  • Recurrent Laryngeal Nerve Injuries
Clinical Trial Details
NCT number NCT04994964
Study type Interventional
Source Birmingham Women's and Children's NHS Foundation Trust
Contact Phil Botha, PhD
Phone +44 121 333 9999
Email p.botha@nhs.net
Status Recruiting
Phase N/A
Start date March 23, 2021
Completion date May 2022
View Details
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