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Compares treatment options for Intubation Complication
Official title Clinical and Economic Comparison of 2 Methods of Intubation Tube Fixation : AnchorFastTM Versus Current Cord Fixation
ClinicalTrials.gov ID: NCT06533436
What this study is testing
- What it's testing
- The aim of this study is to assess the benefits of using the Anchorfast device in reducing complications associated with intubation tube fixation, in terms of the rate of pressure ulcer development, the rate of intubation tube mobilization and the rate of VAP occurrence. If the hypothesis is confirmed, this project would enable the caregivers to optimize the current practice in the interests of both patients and caregivers.
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 18 and older
You may be able to join if
- Patient over 18 years old,
- Patient with orotracheal intubation,
- Patient intubated no more than 24 hours previously,
- Oral consent from patient, trusted support person or relative if unable to consent
- Membership of a French health insurance scheme.
You likely can't join if
- Pre-existing facial, labial or auricular skin lesions,
- Pre-existing mucositis,
- Patients extubated for more than 24 hours whose condition requires a new intubation tube
- Nasotracheal intubation,
- Planned early tracheotomy,
- Patient with occipital craniectomy,
See the full eligibility criteria
- Patient over 18 years old,
- Patient with orotracheal intubation,
- Patient intubated no more than 24 hours previously,
- Oral consent from patient, trusted support person or relative if unable to consent
- Membership of a French health insurance scheme.
- Pre-existing facial, labial or auricular skin lesions,
- Pre-existing mucositis,
- Patients extubated for more than 24 hours whose condition requires a new intubation tube
- Nasotracheal intubation,
- Planned early tracheotomy,
- Patient with occipital craniectomy,
- Patient in ventral position,
- Pregnant or breast-feeding woman,
- Patient deprived of liberty or under guardianship.
The study team makes the final eligibility decision.
Where it's taking place
- Suresnes, France
Compensation & support
Compensation mentioned.
ClinicalTrials.gov doesn't provide a reliable structured field for payment or travel support - confirm details with the study team.
Questions & answers
Do participants get paid in this trial?
This study's listing includes signals that participants may be compensated or receive a stipend. Amounts vary and are set by the study team - confirm the details with them.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.
Who can join this trial?
This study is enrolling all sexes, 18 years and older. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Suresnes, France. Enter your location above to see the nearest site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.