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Correlation of Nasopharyngeal (NP) and Lower Oesophageal (LO) Temperatures in Ventilated Children

NHS Foundation Trust logo

NHS Foundation Trust

Status

Completed

Conditions

Child

Treatments

Device: Nasopharyngeal and oesophageal temperature probes

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

Children lose heat under general anaesthesia, thus temperature is routinely monitored during anaesthesia for all but the shortest cases, and active warming can be used to prevent hypothermia and its resulting complications. Temperature can be measured at several sites dependent on the type of surgery and patient factors. Previously a temperature probe has been sited in the lower third of the oesophagus (swallowing tube) but it is difficult to accurately place this without an X-Ray. Consequently it is more common to use a temperature probe placed in the nasopharynx (where the nose and throat meet), when the child is anaesthetised.

However the investigators do not know if the temperature in the nasopharynx correlates well with the real core temperature or not.This prospective, unblinded, agreement study will seek to find an agreement of 2 methods to measure temperature in children undergoing general anaesthesia with a breathing tube that has a leak.

Full description

It is known that temperature in the lower third of the oesophagus correlates well with the gold standard of core temperature measurement, namely the temperature of blood in the heart. It is not known if oesophageal and nasopharyngeal temperatures correlate in children on a breathing machine via a tube with leak. If this study were to find a good correlation between oesophageal and nasopharyngeal temperature, this would allow clinicians to confidently use the more feasible nasopharyngeal temperature probes.

For this study 100 children will have both nasopharyngeal and oesophageal temperatures measured during general anaesthesia, both in the presence and absence of a leak around the endotracheal tube.

It is hypothesised that even in the presence of a leak, the temperature difference between the two methods will be less than 0.5 degrees centigrade.

Enrollment

59 patients

Sex

All

Ages

8 months to 7 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patient requires general anaesthesia with endotracheal intubation for a procedure assisted by radiography (e.g. line insertion, line change).
  • Patient requires chest radiograph for procedure.
  • Expected anaesthetic time more than 30 minutes.

Exclusion criteria

  • No written parental written consent.
  • Known oesophageal pathology (e.g. tracheo-oesophageal fistula, oesophageal strictures, oesophageal varices, oesophageal atresia).
  • Known base of skull or midface fractures.
  • Previous gastric bypass surgery or nasal surgery.
  • Known coagulopathy.
  • Previous alkaline ingestion.
  • High aspiration risk.
  • Significant respiratory co-morbidity requiring anticipated peak airway pressures > 25 cm of water
  • American Society Anaesthesiologists (ASA) grading 4 - 5.
  • Tracheostomy in situ.
  • Severe sepsis or septic shock or other other condition (such as bronchopulmonary fistula) that precludes use of tidal volume ventilation over 7 ml/kg.
  • Known airway abnormalities (e.g. subglottic stenosis) that preclude placement of a MicroCuff® endotracheal tube.
  • Oesophageal or nasopharyngeal probe contraindicated for reasons related to surgery / procedure.

Trial design

Primary purpose

Supportive Care

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

59 participants in 1 patient group

Nasopharyngeal and oesophageal temperatures
Experimental group
Description:
An oesophageal and nasopharyngeal temperature probe will be placed and temperature will be measured at these site
Treatment:
Device: Nasopharyngeal and oesophageal temperature probes

Trial documents
2

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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