Trials / Completed
CompletedNCT00953433
Laryngeal Morbidity After Endotracheal Intubation - Endoflex-tube Versus Use of Stylet
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 130 (actual)
- Sponsor
- Rigshospitalet, Denmark · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
This study is aimed at reducing the risk of hoarseness and damage to the vocal cords following general anaesthesia. Conventional endotracheal intubation with use of a stylet will be compared with the Endoflex tube. A conventional stylet enforced endotracheal tube is dirigible because of the stiffness gained by the addition of a stylet. In high risk rapid sequence intubation settings the enhanced dirigibility can be crucial, which is why most anaesthesiologists choose to add the stylet in these situations. A new endotracheal tube with a dynamic dirigible end called the Endoflex tube might prove to be a good alternative to the conventional stylet enforced endotracheal tube. Study hypothesis: The Endoflex tube will reduce the risk of hoarseness after intubation when compared to the conventional stylet enforced endotracheal tube under optimal intubation conditions.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Endoflex tube | Size decided upon gender. |
| DEVICE | Polyvinyl chloride endotracheal tube with a stylet | Size decided upon gender. |
Timeline
- Start date
- 2010-04-01
- Primary completion
- 2011-08-01
- Completion
- 2011-08-01
- First posted
- 2009-08-06
- Last updated
- 2011-08-24
Locations
1 site across 1 country: Denmark
Source: ClinicalTrials.gov record NCT00953433. Inclusion in this directory is not an endorsement.