Effect of nasal tracheal tube fixing device on nasal pressure of patients with nasal endotracheal intubation

Status

Recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2100054750

Enrollment

Unknown

Registered

2021-12-26

Start date

2021-08-26

Completion date

Unknown

Last updated

2022-12-05

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

Conditions

Pressure injury

Interventions

experimental group:using nasal tracheal tube fixing device

control group:none

Eligibility

Sex/Gender

All

Age

18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. ASA I-II grade; 2. 18-60 years old; 3. For elective surgery, patients who need general anesthesia with nasotracheal intubation.

Exclusion criteria

Exclusion criteria: 1. Past history of pressure ulcers; 2. Nasal trauma or defect; 3. Secondary intubation due to various reasons (inappropriate intubation size, cuff rupture and intubation failure, etc.); 4. Contraindications for nasotracheal intubation (nasal polyps, nasopharyngeal tumors, epistaxis, laryngeal edema, acute laryngitis, laryngeal submucosal edema, easy bleeding tendency, etc.); 5. Pregnancy; 6. Participated in other relevant clinical investigators within the past 3 months.

Design outcomes

Primary

Measure	Time frame
Nose pressure;	—

Secondary

Measure	Time frame
The incidence of postoperative nasal pressure injury;Nasal comfort 24 hours after surgery;Fixed time required;	—

Countries

China

Contacts

Public ContactXia Ming

Shanghai Ninth People's Hospital

xiaming1980@xzhmu.edu.cn+86 15021306970

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026