NCT Number: NCT00221377
"Cuffed Versus Uncuffed Tracheal Tubes in Small Children"
This randomized controlled multi-centre trial in children from birth up to < 5 years of age aims to demonstrate equivalence as to the major outcome of post-extubation airway injury (stridor) comparing uncuffed tracheal tubes to current tracheal tubes with modern high volume - low pressure cuff combined with a cuff pressure release valve.
Looking for future studies?
Notify MeKey information
Conditions
Age range
1 day–5 year
Sex eligibility
All sexes
Study type
Interventional
Phase
Not applicable
Primary location
Anesthesia And Critical Care Medicine - Medical University, Innsbruck, Austria
About this study
The use of cuffed tracheal tubes is a controversial topic in paediatric anaesthesia and intensive care medicine. Cuffed tubes have traditionally been recommended for children older than 8 to 10 years. During the past decade, however, several authors have argued for the use of cuffed tracheal tubes in younger children and infants. A frequently cited argument against their use is the fear from post-extubation morbidity, allegedly caused by cuff induced tracheal and laryngeal airway injury. Using modern improved designed cuffed tracheal tubes, data from randomised prospective studies, performed in paediatric anaesthesia and intensive care units, suggest that using cuffed tracheal tubes do not carry an increased risk for airway morbidity as compared to uncuffed tracheal tubes in children below 8 years of age if correctly used. However, all these studies are based on single-centre experiences and/or included only a few neonates, infants and small children. Hence, there is equipoise as to the question, whether cuffed tubes are preferable over uncuffed standard tubes.
So, this randomized controlled multi-centre trial in children from birth up to < 5 years of age aims to demonstrate equivalence as to the major outcome of post-extubation airway injury (stridor) comparing uncuffed tracheal tubes to current tracheal tubes with modern high volume - low pressure cuff combined with a cuff pressure release valve.
The primary hypothesis relates to the main outcome criteria of this study, which is post-extubation morbidity as measured by the presence or absence of stridor after tracheal extubation. The null-hypothesis Ho is defined as no difference in the incidence rates of post-extubation morbidity between cuffed and uncuffed groups. The null-hypothesis (Ho: u-Diff = 0) will be compared with the alternative hypothesis (H1: u-Diff <> 0). The study is designed to detect a clinically unacceptable deterioration of 1.5% above the baseline airway-injury rate of 2.5% when using uncuffed tubes with a power of 90% and a type I error probability of less than 5%.
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- Children aged from birth (weighing > 3 kg) to <5 years
- Children requiring oro-tracheal or naso-tracheal intubation with a Magil shaped tracheal tube or preformed (RAE) tracheal tube as a part of their anaesthetic care and planed IPPV during the surgical / interventional / diagnostic procedure
- Tracheal intubation performed using direct laryngoscopy
- Extubation after the procedure in the OR theatre
- Procedure performed in supine position
- Patients for elective and emergency surgery and/or interventions if there is no risk for regurgitation or pulmonary aspiration
- ASA I and II patients
- Written parental consent
Exclusion criteria
- No parental written consent obtained
- Known airway anomalies (airway stenosis, including Down's Syndrome)
- Known or suspected difficult intubation
- Known need for abnormal tube size
- Full stomach and/or at risk for regurgitation
- Surgery of the larynx and/or of the trachea and/or neck and/or upper oesophagus
- Pulmonary diseases (concurrent pneumonia or bronchial infection, asthma requiring inhalation medication, pulmonary malformations)
- ASA class III and higher
- Fiberoptic intubation or alternative intubation technique
- Patients planned for postoperative ventilation in the ICU
- Weight and/or height percentiles < 3% / > 97%
Treatment and study plan
Primary outcomes
-
post-extubation stridor (airway stenosis)
Sponsors and collaborators
Lead sponsor
University Children's Hospital, Zurich
Other
Registry information
Important dates
- Study start
- 2005
- Primary completion
- 2007
- Study completion
- 2007
- First posted
- Sep 22, 2005
- Registry last updated
- May 17, 2012
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Related clinical trials
Published trials that share one or more normalized conditions with this study.
Comparison of Pre-procedure Lignocaine Spray Versus Spray-as-you-go for Topical Airway Anesthesia in Flexible Bronchoscopy
NCT07084623
Airway Disease, Anesthesia, Local
Lahore, Punjab Province, Pakistan
View Trial DetailsUltrasound Assessment of the Larynx and Trachea in the Neonatal Period
NCT05636410
Laryngeal Diseases, Larynx
Krakow, Lesser Poland Voivodeship, Poland
View Trial DetailsUltrasound Evaluation of the Vascular Anatomy of the Neck to Minimize the Accidental Risk of Vascular Puncture During Percutaneous Tracheostomy
NCT06002178
Respiratory Tract Diseases, Trachea
Padova, Veneto, Italy
View Trial DetailsPost-extubation Assessment of Laryngeal Symptoms and Severity
NCT03726086
Complication of Ventilation Therapy, Critical Illness
Baltimore, Maryland, United States
View Trial Details