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Comparison for the time required of nasotracheal intubation assisted by cuff inflation method and Magill forceps

Comparison for the time required of nasotracheal intubation assisted by cuff inflation method and Magill forceps

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200057304
Enrollment
Unknown
Registered
2022-03-07
Start date
2022-06-01
Completion date
Unknown
Last updated
2023-10-09

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

Conditions

Nasal tracheal intubation

Interventions

Experimental group:Nasal tracheal intubation with cuff inflation
Control group:Magill forceps

Sponsors

The First Affiliated Hospital of Anhui Medical University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Patients under general anesthesia for nasal tracheal intubation, aged 18-64 years, regardless of gender; 2. BMI 18-30 kg/m2; 3. Normal communication; 4. ASA grade I-II; 5. Signed informed consent.

Exclusion criteria

Exclusion criteria: 1. Severe cardiopulmonary system diseases; 2. Endocrine system diseases: pituitary tumor, severe diabetes, increased cortisol syndrome, pheochromocytoma and other; 3. Mental diseases: Schizophrenia, depression, chronic analgesic drug use, alcoholism, opioid dependence, Parkinson's disease, cerebral infarction; 4. Alzheimer's disease, severe insomnia; 5. Inability to understand 15-item Quality of Recovery (QOR-15); 6. Preoperative life was not able to take care of themselves; 7. Hemorrhagic disease history or abnormal coagulation function; 8. Patients with curved nasal passages and narrow nasal passages.

Design outcomes

Primary

MeasureTime frame
Time required for intubation;

Secondary

MeasureTime frame
Tissue damage;15-item Quality of Recovery, QoR-15;Hemodynamic parameters;Adverse reaction;

Countries

China

Contacts

Public ContactLu Yao

The First Affiliated Hospital of Anhui Medical University

luyao-mz@163.com+86 18956564060

Outcome results

None listed

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