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Clinical trials for Intubation

The European Union Clinical Trials Register   allows you to search for protocol and results information on:
  • interventional clinical trials that were approved in the European Union (EU)/European Economic Area (EEA) under the Clinical Trials Directive 2001/20/EC
  • clinical trials conducted outside the EU/EEA that are linked to European paediatric-medicine development

    • EU/EEA interventional clinical trials approved under or transitioned to the Clinical Trial Regulation 536/2014 are publicly accessible through the
    Clinical Trials Information System (CTIS).

    The EU Clinical Trials Register currently displays   43871   clinical trials with a EudraCT protocol, of which   7290   are clinical trials conducted with subjects less than 18 years old.   The register also displays information on   18700   older paediatric trials (in scope of Article 45 of the Paediatric Regulation (EC) No 1901/2006).

    Phase 1 trials conducted solely on adults and that are not part of an agreed paediatric investigation plan (PIP) are not publicly available (see Frequently Asked Questions ).  
     
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    318 result(s) found for: Intubation. Displaying page 1 of 16.
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    EudraCT Number: 2010-021887-13 Sponsor Protocol Number: NL32588.075.10 Start Date*: 2010-11-04
    Sponsor Name:Isala Clinics Zwolle
    Full Title: Detection of stress in newborns during intubation by means of skin conductance measurements.
    Medical condition: respiratory insufficiency
    Disease: Version SOC Term Classification Code Term Level
    12.1 10067450 Endotracheal intubation LLT
    Population Age: Preterm newborn infants, Newborns, Under 18 Gender: Male, Female
    Trial protocol: NL (Ongoing)
    Trial results: (No results available)
    EudraCT Number: 2009-014256-30 Sponsor Protocol Number: HU08/NEONAT/REMIFENTANIL Start Date*: 2009-09-11
    Sponsor Name:Hôpital Universitaire Des Enfants Reine Fabiola
    Full Title: Une analgésie de choix pour l'intubation des nouveau-nés : Etude multicentrique randomisée comparant le rémifentanil à l'association morphine-midazolam
    Medical condition: Preterm newborn & newborm requiring an elective endotacheal intubation
    Disease: Version SOC Term Classification Code Term Level
    12.0 10067450 Endotracheal intubation LLT
    Population Age: Preterm newborn infants, Newborns, Under 18 Gender: Male, Female
    Trial protocol: BE (Ongoing)
    Trial results: (No results available)
    EudraCT Number: 2012-002648-26 Sponsor Protocol Number: S54472 Start Date*: 2013-10-16
    Sponsor Name:UZ Leuven
    Full Title: Exploratory Propofol Dose Finding Study In Neonates.
    Medical condition: Investigation of the most effective intravenously administered single propofol dose for successful INSURE prodecure and for (semi-)elective intubation of neonates in non-INSURE conditions (e.g. sur...
    Disease: Version SOC Term Classification Code Term Level
    16.0 100000004869 10028977 Neonate LLT
    16.0 10042613 - Surgical and medical procedures 10067450 Endotracheal intubation PT
    16.0 10042613 - Surgical and medical procedures 10049124 Sedation during medical procedure LLT
    16.0 10022891 - Investigations 10061134 Drug level therapeutic PT
    Population Age: Preterm newborn infants, Newborns, Under 18 Gender: Male, Female
    Trial protocol: BE (Completed)
    Trial results: (No results available)
    EudraCT Number: 2009-014885-25 Sponsor Protocol Number: CHIC001 Start Date*: Information not available in EudraCT
    Sponsor Name:Centre Hospitalier Intercommunal de Créteil
    Full Title: PRETTINEO PREmedication Trial for Tracheal Intubation of the NEOnate
    Medical condition: Comparison of two premedication regimens for semi-elective or elective intubation of newborns (term and preterm) hospitalized in the NICU
    Disease: Version SOC Term Classification Code Term Level
    13.1 10042613 - Surgical and medical procedures 10067450 Endotracheal intubation PT
    13.1 10042613 - Surgical and medical procedures 10036500 Premedication PT
    Population Age: Preterm newborn infants, Newborns, Under 18 Gender: Male, Female
    Trial protocol: FR (Ongoing)
    Trial results: View results
    EudraCT Number: 2017-000704-26 Sponsor Protocol Number: ONSD5 Start Date*: 2018-08-10
    Sponsor Name:
    Full Title: Influence of Endotracheal Intubation versus Endotracheal Intubation with Lidocaine on Intracranial Pressure assessed by Optic Nerve Sheath Diameter
    Medical condition: Patients undergoing surgery at the Erasmus Medical Centre Rotterdam in a period from January 2018 till the end of inclusion.
    Disease:
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: NL (Ongoing)
    Trial results: (No results available)
    EudraCT Number: 2004-001583-52 Sponsor Protocol Number: Intu Start Date*: 2004-09-22
    Sponsor Name:Lund University Hospital
    Full Title: Balanced anestesia for intubation of newborn premature infants – a randomized intervention study Balanserad anestesi för intubation av nyfödda prematura barn – en randomiserad interventionsstudie
    Medical condition: Respiratory insufficiency in prematrue infants requiring ventilatory assistance and therefore intubation. Premedication before intubation.
    Disease:
    Population Age: Preterm newborn infants, Newborns, Under 18 Gender: Male, Female
    Trial protocol: SE (Completed)
    Trial results: View results
    EudraCT Number: 2021-000727-12 Sponsor Protocol Number: RC31/20/0443 Start Date*: 2021-06-28
    Sponsor Name:University Hospital of Toulouse
    Full Title: Quality Assessment of Tracheal intubation without neuromuscular blocking drugs (Propofol+ Remifentanil) in obese patients: Pilot Study
    Medical condition: induction phase of the general anesthesia in obese patients
    Disease:
    Population Age: Adults Gender: Male, Female
    Trial protocol: FR (Completed)
    Trial results: (No results available)
    EudraCT Number: 2021-000691-11 Sponsor Protocol Number: 89303200 Start Date*: 2022-01-18
    Sponsor Name:Rigshospitalet
    Full Title: Comparison of the effect of xylometazoline and cocaine on epistaxis when administered as local vasoconstrictors prior to nasal intubation
    Medical condition: Epistaxis upon nasal intubation
    Disease:
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: DK (Completed)
    Trial results: (No results available)
    EudraCT Number: 2011-003216-23 Sponsor Protocol Number: UF8736 Start Date*: Information not available in EudraCT
    Sponsor Name:CHRU MONTPELLIER
    Full Title: Intranasal Midazolam versus intranasal Ketamine to sedate newborns for intubation in delivery room
    Medical condition: Maladie des membranes hyalines du nouveau-né (Code CIM : P22.OX-001)
    Disease:
    Population Age: Preterm newborn infants, Under 18 Gender: Male, Female
    Trial protocol: FR (Completed)
    Trial results: (No results available)
    EudraCT Number: 2005-000877-23 Sponsor Protocol Number: JM/JS/4551 Start Date*: 2005-04-11
    Sponsor Name:Oxford Radcliffe Hospitals NHS trust
    Full Title: Is Remifentanil better than Propofol in providing optimal conditions for an awake fibreoptic intubation?
    Medical condition: Awake fibre optic intubation is an anaesthetic technique used to intubate patients with a difficult to manage airway. It s a procedure by which a tracheal tube is inserted in a patients trachea wh...
    Disease:
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: GB (Completed)
    Trial results: View results
    EudraCT Number: 2004-004728-11 Sponsor Protocol Number: MR/EUM202 Start Date*: 2005-03-25
    Sponsor Name:Avera Pharmaceuticals Inc.
    Full Title: A Multicenter, Randomized, Controlled, Observer-Blinded, Dose-Response Study to Evaluate The Efficacy in Tracheal Intubation and Safety of Gantacurium Chloride for Injection in Healthy Adult Patien...
    Medical condition: Adjunct to anesthesia to facilitate tracheal intubation (non-depolarizing neuromuscular blocking agent)
    Disease:
    Population Age: Adults Gender: Male, Female
    Trial protocol: GB (Completed) DE (Completed) DK (Completed)
    Trial results: (No results available)
    EudraCT Number: 2011-000790-31 Sponsor Protocol Number: 2011-000790-31 Start Date*: 2011-04-29
    Sponsor Name:AZIENDA UNIVERSITARIA POLICLINICO UMBERTO I DI ROMA
    Full Title: Propofol-based or Sevoflurane-based Anesthesia Induction in Patients Undergoing Fiberoptic Tracheal Intubation for Cervical Spine Surgery: Effects on Systemic Hemodynamics and Respiratory Drive- th...
    Medical condition: surgery for cervical myelopathy
    Disease:
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: IT (Ongoing)
    Trial results: (No results available)
    EudraCT Number: 2019-000753-31 Sponsor Protocol Number: RC19_0055 Start Date*: 2019-07-04
    Sponsor Name:CHU Nantes
    Full Title: Evaluation of REMIFENTANIL as an alternative to curare for rapid sequence anesthetic induction in patients at risk of gastric fluid inhalation
    Medical condition: anesthetic induction
    Disease: Version SOC Term Classification Code Term Level
    20.0 100000004865 10002326 Anesthetic induction LLT
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: FR (Completed)
    Trial results: View results
    EudraCT Number: 2009-018169-12 Sponsor Protocol Number: Local/2009/AC-02 Start Date*: 2010-10-01
    Sponsor Name:CHU de Nîmes
    Full Title: Etude randomisée évaluant l’efficacité et la tolérance du rémifentanil lors d’une induction en séquence rapide, chez des sujets fragiles
    Medical condition: Anesthésie
    Disease:
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: FR (Completed)
    Trial results: (No results available)
    EudraCT Number: 2012-001671-36 Sponsor Protocol Number: EC11-103 Start Date*: 2012-08-27
    Sponsor Name:Fundación para la Investigación Biomédica
    Full Title: A phase IV randomized, controlled clinical trial to compare the high flow oxygen therapy (group of intervention) opposite to the conventional oxygen therapy (group control) in patients with severe ...
    Medical condition: Severe acute respiratory failure
    Disease:
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: ES (Completed)
    Trial results: View results
    EudraCT Number: 2020-001767-86 Sponsor Protocol Number: COVIRL-002 Start Date*: 2020-06-25
    Sponsor Name:University College Dublin
    Full Title: An open-label, multi-centre, randomised trial comparing different doses of single-dose tocilizumab in adults with severe, non-critical, PCR-confirmed COVID-19 infection with evidence of progressive...
    Medical condition: COVID-19 infection
    Disease: Version SOC Term Classification Code Term Level
    23.0 10021881 - Infections and infestations 10051905 Coronavirus infection PT
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: IE (Prematurely Ended)
    Trial results: (No results available)
    EudraCT Number: 2009-013283-39 Sponsor Protocol Number: 2009-13 Start Date*: 2009-10-07
    Sponsor Name:Assistance publique hôpitaux de marseille
    Full Title: sevofluorane versus propofol pour l'intubation des nouveau-nés en réanimation
    Medical condition: nouveau-nés en réanimation pédiatrique.
    Disease:
    Population Age: Preterm newborn infants, Newborns, Under 18 Gender: Male, Female
    Trial protocol: FR (Ongoing)
    Trial results: (No results available)
    EudraCT Number: 2013-005572-17 Sponsor Protocol Number: 20132312 Start Date*: 2014-05-21
    Sponsor Name:Erasmus Medical Center
    Full Title: Optimizing propofol dosing for (preterm) newborn infants that need endotracheal intubation
    Medical condition: Sedation for endotracheal intubation in newborns of different ages at the neonatal intensive care unit
    Disease: Version SOC Term Classification Code Term Level
    16.1 100000004869 10029392 Newborn LLT
    Population Age: Preterm newborn infants, Newborns, Under 18 Gender: Female
    Trial protocol: NL (Ongoing)
    Trial results: (No results available)
    EudraCT Number: 2021-002824-19 Sponsor Protocol Number: NA Start Date*: 2021-08-12
    Sponsor Name:CHU de Liège
    Full Title: Study of the hypnotic and anti-nociceptive components of Magnesium using Electroencephalogram Spectral Entropy and pupillometry during total intravenous general anesthesia : a randomized double-bli...
    Medical condition: Total thyroidectomy
    Disease:
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: BE (Ongoing)
    Trial results: (No results available)
    EudraCT Number: 2020-005384-31 Sponsor Protocol Number: RSIv80 Start Date*: 2021-03-19
    Sponsor Name:Rigshospitalet
    Full Title: A single blinded multicenter randomized study comparing intubating conditions during rapid sequence induction with either suxamethonium 1.0 mg/kg or rocuronium 1.0 mg/kg in elderly patients (≥ 80 y...
    Medical condition: The aim of this study is to determine the proportion of excellent tracheal intubation conditions at 60 seconds after administration of either rocuronium 1.0 mg/kg or suxamethonium 1 mg/kg in patien...
    Disease: Version SOC Term Classification Code Term Level
    23.1 100000004865 10051079 Orthopedic procedure LLT
    20.0 100000004856 10000082 Abdominal pain generalised LLT
    Population Age: Elderly Gender: Male, Female
    Trial protocol: DK (Ongoing)
    Trial results: (No results available)
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    The status and protocol content of GB trials is no longer updated since 1 January 2021. For the UK, as of 31 January 2021, EU Law applies only to the territory of Northern Ireland (NI) to the extent foreseen in the Protocol on Ireland/NI. Legal notice
    As of 31 January 2023, all EU/EEA initial clinical trial applications must be submitted through CTIS . Updated EudraCT trials information and information on PIP/Art 46 trials conducted exclusively in third countries continues to be submitted through EudraCT and published on this website.

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