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Endotracheal intubation in elective cervical surgery: A randomised, controlled, assessor-blinded study

Endotracheal intubation in elective cervical surgery: A randomised, controlled, assessor-blinded study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-INR-16008070
Enrollment
Unknown
Registered
2016-03-08
Start date
2014-02-01
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

Cervical spondylosis

Interventions

GS group:endotracheal intubation using the GS video laryngoscope (GS group)
LMA group:endotracheal intubation using the CTrach LMA (LMA group)
SOS group:endotracheal intubation using the SOS rigid laryngoscope (SOS group)

Sponsors

Shenyang Military Command General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: The inclusion criteria were: aged between 18 and 65 years; body mass index (BMI) 20-30 kg/m2; American Society of Anesthesiology (ASA) physical status class I or II; and New York Heart Association functional classification grade I or II.

Exclusion criteria

Exclusion criteria: The exclusion criteria were: mouth opening < 3 cm, thyromental distance < 6.5 cm, or micrognathia; a positive pregnancy test for a woman of child-bearing potential; previously medicated with any cardiovascular-active agent; complicating uncontrolled diabetes mellitus or serious cardiopulmonary or hepatorenal impairment; or, rejecting participation in the study.

Design outcomes

Primary

MeasureTime frame
changes in the Cobb angles;—

Countries

China

Contacts

Public ContactZhang Tiezheng

Shenyang Military Command General Hospital

tzzhang@hotmail.com+86 13309884069

Outcome results

None listed

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