Informazioni generali
  • Categoria della malattia Gravidanza e parto , Malattie delle vie respiratorie (non cancro) (BASEC)
  • Stato di reclutamento reclutamento in corso (BASEC/ICTRP)
  • Luogo dello studio
    Aarau, Berna, Ginevra, Losanna, Luzern
    (BASEC)
  • Responsabile dello studio PD Dr. med. Alexander Fuchs alexander.fuchs@insel.ch (BASEC)
  • Fonte dati BASEC: Importato da 11.07.2025 ICTRP: N/A
  • Ultimo aggiornamento 11.07.2025 20:15
HumRes63231 | SNCTP000005639 | BASEC2023-00881

Oxygen with different flow rates during the placement of the ventilation tube in newborns and infants - a multicenter, non-inferiority, prospective, randomized controlled study

  • Categoria della malattia Gravidanza e parto , Malattie delle vie respiratorie (non cancro) (BASEC)
  • Stato di reclutamento reclutamento in corso (BASEC/ICTRP)
  • Luogo dello studio
    Aarau, Berna, Ginevra, Losanna, Luzern
    (BASEC)
  • Responsabile dello studio PD Dr. med. Alexander Fuchs alexander.fuchs@insel.ch (BASEC)
  • Fonte dati BASEC: Importato da 11.07.2025 ICTRP: N/A
  • Ultimo aggiornamento 11.07.2025 20:15

Descrizione riassuntiva dello studio

Oxygen is vital for survival. With each breath, our body is supplied with it. However, during general anesthesia, autonomous breathing (so-called apnea) is stopped. Particularly in infants and newborns, lack of oxygen can lead to hypoxia and cardiac arrest in a very short time. To prevent this, patients under general anesthesia are ventilated with a ventilation mask until the ventilation tube is placed in the trachea (so-called intubation) and artificial ventilation is started via a ventilator. During the actual placement of the ventilation tube, ventilation with the ventilation mask is not possible. • In previous studies, we have shown that the administration of additional oxygen via a nasal cannula without autonomous breathing (so-called apneic oxygenation) significantly prolongs the time until hypoxia occurs in the body. However, it is currently unclear what the flow rate of the oxygen should be. • The aim of the study is to investigate the optimal oxygen flow rate during the placement of the ventilation tube into the trachea of newborns and infants in the operating room. To do this, we compare a low and a high oxygen flow rate during apnea. These two flow rates have been shown to be safe and effective in previous studies.

(BASEC)

Intervento studiato

At the beginning, the procedure is the same as for any operation. The children are received by a specialized anesthesia team. A sensor for measuring oxygen in the blood is attached to the child's finger or toes, a blood pressure cuff is placed on the arm, and electrodes for cardiac monitoring are attached to the chest. The anesthesia team will establish venous access. Anesthesia will be started with the usual medications after oxygen has been administered to the child for 1 minute. The child will be ventilated for one minute with a ventilation mask until all medications have taken full effect. Meanwhile, the study team will open an envelope to learn the random assignment of your child.

 

Low oxygen flow: 100% oxygen, flow rate 0.2 L/kg/min, conventional nasal cannula

or

High oxygen flow: 100% oxygen, flow rate 2 L/kg/min with Optiflow device.

Once the oxygen supply is installed, intubation will be performed with a laryngoscope with camera (videolaryngoscopy). This corresponds to the standard procedure. After the placement of the ventilation tube in the trachea, the study is completed and the intervention or examination can begin. If the placement of the ventilation tube in the trachea fails on the first attempt, a maximum of two additional attempts will be made. In this case, the anesthesia team is free to change the oxygen flow rate and/or perform the placement of the ventilation tube in the trachea with another device. If the placement of the ventilation tube in the trachea continues to be unsuccessful, we will follow the standardized treatment pathway for a difficult airway. In all cases, the data and measurements will be recorded, and the child will be visited 24 hours after the operation by an anesthesiologist to identify any complications.

(BASEC)

Malattie studiate

The aim of this study is to investigate the optimal oxygen flow rate required during intubation with the C-MAC videolaryngoscope (Karl Storz, Tuttlingen, Germany) in the operating room or in the intensive care unit. We assume that the difference between low-flow and high-flow oxygen supply is negligible.

(BASEC)

Criteri di partecipazione
Inclusion criteria: • the child is, calculated from the date of conception, not older than 52 weeks. • the child requires a planned, urgent, or emergency placement of the ventilation tube in the trachea (intubation) for a surgical procedure/a non-surgical intervention under general anesthesia. (BASEC)

Criteri di esclusione
Exclusion criteria: • If the child has a known disease or malformation that could complicate airway management and therefore requires a technique other than videolaryngoscopy for airway securing. • If the child requires intubation due to an acute heart or lung disease. • If the child has a congenital heart disease where 100% oxygen cannot be used. (BASEC)

Luogo dello studio

Aarau, Berna, Ginevra, Losanna, Luzern

(BASEC)

non disponibile

Sponsor

Inselspital Bern

(BASEC)

Contatto per ulteriori informazioni sullo studio

Persona di contatto in Svizzera

PD Dr. med. Alexander Fuchs

+41 31 632 5201

alexander.fuchs@insel.ch

Inselspital Bern

(BASEC)

Informazioni scientifiche

non disponibile

Nome del comitato etico approvante (per studi multicentrici solo il comitato principale)

Commissione d'etica Berna

(BASEC)

Data di approvazione del comitato etico

10.07.2023

(BASEC)


ID di studio ICTRP
non disponibile

Titolo ufficiale (approvato dal comitato etico)
LaryngOscoPy for neonaTal and Infant aIrway Management wIth Supplemental oxygEn at different flow rates (OPTIMISE-2): a multi-center, non-inferiority, prospective randomized controlled trial (BASEC)

Titolo accademico
non disponibile

Titolo pubblico
non disponibile

Malattie studiate
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Intervento studiato
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Tipo di studio
non disponibile

Disegno dello studio
non disponibile

Criteri di inclusione/esclusione
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non disponibile

Endpoint primari e secondari
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Data di registrazione
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Inclusione del primo partecipante
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Sponsor secondari
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Contatti aggiuntivi
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ID secondari
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Risultati-Dati individuali dei partecipanti
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Ulteriori informazioni sullo studio
non disponibile

Risultati dello studio

Riepilogo dei risultati

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Link ai risultati nel registro primario

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