Trials / Unknown
UnknownNCT05415059
LEAFix Adhesion in Healthy Volunteers
Laryngeal, Endotracheal Airway Fixator (LEAFix): In Vivo Skin Adhesion Verification Protocol
- Status
- Unknown
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 32 (estimated)
- Sponsor
- Liverpool University Hospitals NHS Foundation Trust · Other Government
- Sex
- All
- Age
- 18 Years – 65 Years
- Healthy volunteers
- Accepted
Summary
This study compares the adhesiveness of the 3M material to be used in the final design.
Detailed description
The material is taken from a CE marked stoma bag. Strips will be placed on to healthy volunteers on the arm and face for 10 minutes and 24 hours. A force gauge will measure the peel force. This will be compared to previous testing on metal. Participants will also be assessed and followed up for any adverse skin issues.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Covatech Stoma bag material | Strips of Covatech Stoma bag used to asses adhesion of 3M material to be used in LEAFix device |
Timeline
- Start date
- 2022-08-10
- Primary completion
- 2022-10-01
- Completion
- 2022-11-01
- First posted
- 2022-06-10
- Last updated
- 2022-08-08
Source: ClinicalTrials.gov record NCT05415059. Inclusion in this directory is not an endorsement.