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Factors predicted with Endotracheal tube and securement method associated skin injury (ETTASMASI) among critical ill patients.

Factors predicted with Endotracheal tube and securement method associated skin injury (ETTASMASI) among critical ill patients.

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
TCTR
Registry ID
TCTR20210426001
Enrollment
165
Registered
2021-04-26
Start date
2021-02-16
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

An endotracheal tube (ETT) is a one of medical devices for a patient with multi organ failure who needed respiratory assistance from a ventilator to maintain breathing and oxygenate the blood in the brain, chest, respiratory tract and the lungs. However, the ETT can cause harm, which means that there is a balance between benefit and harm. ETTs are often an essential component in delivering necessary care to critically ill patients, yet are many potential complications during ETT intubation, i

Interventions

The critically ill patients requiring endotracheal intubation and mechanical ventilation for at least 24 hours who should be over 18 years of age, there should be ETT use with secure methods includin
Basic Science
The mechanically ventilated patients in an acute care setting in Srinagarind Hospital

Sponsors

Faculty of Medicine, Khon Kaen University, Thailand
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 100 Years

Inclusion criteria

Inclusion criteria: The inclusion criteria stipulated that 1) participants should be > 18 years of age, 2) there should be ETT use with secure methods including adhesive tape, gauze tying, or cloth tape tying among critical ill patients requiring endotracheal intubation and mechanical ventilation for at least 24 hours, 3) 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
Lip ulcer, ear ulcer, and facial skin injury plan extubation Stage I: skin with erythema Stage II: partial loss of skin Stage III: loss of skin in its overall thickness; and Stage IV: loss of skin in its total thickness and tissue loss.

Secondary

MeasureTime frame
N/A N/A N/A

Countries

Thailand

Contacts

Public ContactTeerawat Somkamsri

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