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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03056820
Other study ID # 12197
Secondary ID
Status Completed
Phase N/A
First received January 27, 2017
Last updated February 14, 2017
Start date May 2010
Est. completion date March 2011

Study information

Verified date February 2017
Source University of Kansas Medical Center
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to compare the effect of the 25° head-up position versus the 55° head-up position on tolerable apnea time (TAT) after induction of general anesthesia in patients with a body mass index (BMI) of 30-40.


Recruitment information / eligibility

Status Completed
Enrollment 74
Est. completion date March 2011
Est. primary completion date March 2011
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- American Society of Anesthesiologists (ASA) physical status I-III

- Body Mass Index (BMI) of 30-40

- Scheduled for an elective surgery that requires tracheal intubation

Exclusion Criteria:

- Patients with abnormalities of the upper airway that require awake tracheal intubation

- Asthma

- Chronic obstructive pulmonary disease

- Congestive heart failure

- Pregnant patients

Study Design


Related Conditions & MeSH terms


Intervention

Other:
25° head-up position
Participant will be positioned at 25° angle for procedure.
55° head-up position
Participant will be positioned at 55° angle for procedure.

Locations

Country Name City State
United States University of Kansas Medical Center Kansas City Kansas

Sponsors (1)

Lead Sponsor Collaborator
University of Kansas Medical Center

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Tolerable Apnea Time (TAT) Measure of the TAT between groups to determine if the TAT is a function of the participant's position. Time between start of induction of general anesthesia (SpO2 100%) to decline of SpO2 94%, up to eight minutes
Secondary Length of time to intubation (TTI) Time between start of the tracheal intubation procedure to completion of tracheal intubation, up to 2 minutes
Secondary Peripheral arterial hemoglobin oxygen saturation (SpO2) trough Measure of the rebound SpO2. It is the lowest SpO2 reading reached subsequent to start of mechanical ventilation at the SpO2 value of 94% and it represents final completion of SpO2 decline. Time until SpO2 decreased to 92%, up to 8 minutes
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