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Study on a self-developed mask type endotracheal intubation fixation device for preventing pressure injury

Comparison of the fixation effect of self-developed mask endotracheal tube fxation device and traditional endotracheal tube fxation device: a randomised controlled study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300078132
Enrollment
Unknown
Registered
2023-11-29
Start date
2022-11-01
Completion date
Unknown
Last updated
2023-12-03

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

Conditions

Endotracheal intubation-related pressure injury

Interventions

Treatment group:Self-developed mask type endotracheal intubation fixation device
Control group:Disposable endotracheal intubation fixator

Sponsors

Nanjing Lishui People's Hospitial (Zhongda Hospital Lishui Branch, Southeast University)
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 95 Years

Inclusion criteria

Inclusion criteria: (1)Age = 18 years old; (2)Meeting the indications for endotracheal intubation; (3)Sign informed consent form by patient or family members.

Exclusion criteria

Exclusion criteria: (1) Patients who are not suitable for oral tracheal intubation; (2) Patients with damaged lips, facial skin, and oral mucosa before intubation; (3) Patients who are not suitable for wearing headbands.

Design outcomes

Primary

MeasureTime frame
Incidence of pressure injury related to endotracheal intubation;—

Secondary

MeasureTime frame
Rate of endotracheal tube dislodgement;Incidence of ventilator-associated pneumonia;Duration of mechanical ventilation;—

Countries

China

Contacts

Public ContactZhang Qibing

Nanjing Lishui People's Hospitial (Zhongda Hospital Lishui Branch, Southeast University)

zhangqibing@lsrmyy.com+86 177 1419 6890

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 6, 2026