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A quasi-experimental study to compare the effectiveness and incidence of endotracheal tube and securement method related skin injury (ETTSM-RSI) between adhesive tape and endotracheal tube fastener in critically ill patients

A quasi-experimental study to compare the effectiveness and incidence of ETTSM-RSI between adhesive tape and endotracheal tube fastener in critically ill patients

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
TCTR
Registry ID
TCTR20211123001
Enrollment
80
Registered
2021-11-23
Start date
2021-12-01
Completion date
Unknown
Last updated
2026-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

endotracheal tube and securement method related skin injury (ETTSM-RSI) were reported between 6.2% and 45%. Recent studies were shown that the AnchorFast oral endotracheal tube fastener can effectively decrease ETTSM-RSI. However, there are no studies using the AnchorFast oral endotracheal tube fastener in patients with edema, acute or chronic renal failure, or vasopressor used. The aim of this study is (1) to evaluate the effectiveness between adhesive tape versus endotracheal tube fastene

Interventions

The AnchorFast oral endotracheal tube fastener combines a number of features that make it the right choice. It is designed to help prevent the formation of lip and fecial skin ulcers through the use o
Experimental Device,No Intervention No treatment
The AnchorFast oral endotracheal tube fastener ,standard care

Sponsors

Invitation Research fund, faculty of medicine, Khon Kaen University, Thailand
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 100 Years

Inclusion criteria

Inclusion criteria: participants should be > 18 years of age, 2) there should be ETT use orotracheal intubation and mechanical ventilation for at least 24 hours, 3) they must be edema, acute or chronic renal failure, or vasopressor used. 4) consent for participation from patient family members should be provided.

Exclusion criteria

Exclusion criteria: Patients were excluded if they (1) were intubated greater than 24 hours prior to admission to this setting, (2) had lip ulcer or facial skin breakdown prior to enrollment, and (3) required nasotracheal intubation, or (4) had a documented allergy to tape.

Design outcomes

Primary

MeasureTime frame
skin injurise untill extubation NPUAP pressure injury staging system

Secondary

MeasureTime frame
Endotracheal tube slippage untill extubation Endotracheal tube slippage scale

Countries

Thailand

Contacts

Public Contactteerawat somkamsri

Srinagarind hospital, Faculty of medicine, Khon Kaen University, Thailand

teeraso@kku.ac.th0863878005

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026