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Comparison of the effects of plastic membrane-isolated fiberscope-guided nasotracheal intubation

Comparison of the effects of plastic membrane-isolated fiberscope-guided nasotracheal intubation

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500095115
Enrollment
Unknown
Registered
2025-01-02
Start date
2025-01-15
Completion date
Unknown
Last updated
2025-01-06

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

Conditions

Epistaxis caused by nasotracheal tube

Interventions

Experimental group:Plastic membrane assists in nasotracheal intubation isolation after general anesthesia
Control group:Routine nasotracheal intubation after general anesthesia

Sponsors

Second Xiangya Hospital of CSU
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. ASA graded as Class I or II; 2. Age>=18 years; 3. Elective oral and maxillofacial surgery; 4. Voluntarily sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. History of previous nasal surgery or trauma; 2. Recurrent epistaxis; 3. Coagulation function is abnormal or anticoagulant therapy is underway; 4. Anticipated difficult intubation; 5. Other patients who are not suitable for clinical trials.

Design outcomes

Primary

MeasureTime frame
Epistaxis;

Secondary

MeasureTime frame
Intubation Characteristics;

Countries

China

Contacts

Public ContactXu Junmei

The Second Xiangya Hospital, Central South University

13975148864@139.com+86 731 85292476

Outcome results

None listed

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