Skin Conductance in Ventilated Preterms

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age22+
SponsorUppsala University Hospital

About this trial

The goal of this observational study is to learn more about the pain and stress experienced by newborn infants receiving mechanical ventilation (breathing through a machine).

The main questions it aims to answer are:

* Do different ventilator settings (modi) cause different degrees of pain and stress? * Can skin conductance measurement be used to evaluate the pain and stress caused by mechanical ventilation in newborns? * Can skin-to-skin care alleviate the stress caused by mechanical ventilation?

Participants will be monitored according to clinical protocol with the addition of electrodes placed on the infant's foot, measuring changes in skin conductance.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Need for mechanical ventilation

Disqualifiers

Other distracting painful conditions

Facial malformation or neuromuscular disease, not allowing regular visual pain assessment

Trial design

Design model

Sequential

Treatments tested in this trial

  • Skin Conductance Measurement

    Device

    Objectifying stress by measuring changes in skin conductance using electrodes placed on the infants' feet.

Treatment groups

No treatment groups listed

Trial outcomes

Primary outcomes

1

Changes in skin conductance

Changes in skin conductance measured in micro Siemens

Time frame
From the time on one ventilator setting to another, on average about two weeks

Secondary outcomes

Other outcomes

Sponsors and contacts

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