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Visual laryngoscope intubation application in normal airway: a prospective, randomized, single-blind controlled clinical study

Clinical research and promotion of visual endotracheal intubation

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IOR-16009023
Enrollment
Unknown
Registered
2016-08-14
Start date
2016-08-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

elective surgery

Interventions

groupG:visual laryngoscope intubation
groupM:traditional direct laryngoscope

Sponsors

Anesthesia department of the affiliated hospital of zunyi Medical college
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. aged 18 years to 65 years old; 2. Requirement for elective surgery, and tracheal intubation for general anesthesia; 3. ASA I - III.

Exclusion criteria

Exclusion criteria: 1. Patients with neck injury determined before operation, who need special tracheal intubation; 2. Patients who have been involved in other clinical trials within the latest 3 months; 3. Patients who are believed not suitable to establish airway with the intubation involved in this research. End point: 1. Patients change operation, anesthesia and intubation methods due to the condition needs; 2. Airway ventilation condition changes, which may endanger patients ventilation.

Design outcomes

Primary

MeasureTime frame
success rate of intubation;intubation-related complications;intubation time;coincidence rate of trachea tube shaping angle;

Secondary

MeasureTime frame
exposure time of glottis;

Countries

China

Contacts

Public ContactLiu Dexing

Affiliated hospital of Zunyi Medical College

pokowenl@163.com+86 15120385331

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Mar 3, 2026