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Different methods used for fiberoptic intubation

Different methods used for fiberoptic intubation

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100043560
Enrollment
Unknown
Registered
2021-02-21
Start date
2021-03-01
Completion date
Unknown
Last updated
2021-06-14

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

Conditions

Fiberoptic intubation

Interventions

Pair Team:Double operation
Single operation group:Single operation

Sponsors

Plastic surgery hospital of Chinese Academy of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. American Society of anesthesiologists (ASA) grade I-II; 2. For the subjects aged 18-55, the normal range of body mass index was 18.5-23.9kg/m2; 3. The patients without respiratory and circulatory complications had normal liver, kidney and lung functions; 4. All patients were operated under general anesthesia; 5. Subjects who can provide written informed consent and patients who can complete the research requirements.

Exclusion criteria

Exclusion criteria: 1. Patients with a history of respiratory tract infection within 2 weeks; 2. Subjects with oral and otorhinolaryngological diseases and surgical history; 3. Patients with connective tissue disease; 4. Diabetic patients; 5. Patients with severe airway difficulties expected; 6. Subjects with reading or communication disabilities; 7. Patients considered unsuitable by other researchers for clinical study.

Design outcomes

Primary

MeasureTime frame
Intubation success rate;Time required for intubation;Hemodynamics;

Secondary

MeasureTime frame
Intubation complications;

Countries

China

Contacts

Public ContactAn Jie

Plastic Surgery Hospital of Chinese Academy of Medical Sciences

ange0721@163.com+86 15801626150

Outcome results

None listed

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