Evaluation of Apnea Tolerance in Bariatric Patients Following Rapid-sequence Induction of Anesthesia

NCT ID: NCT03056807

Last Updated: 2017-02-17

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

65 participants

Study Classification

INTERVENTIONAL

Study Start Date

2008-10-31

Study Completion Date

2011-08-31

Brief Summary

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The purpose of this study is to compare the effect of the 25° head-up position versus the 55° head-up position on tolerable apneic time (TAT) in bariatric patients scheduled for laparoscopic adjustable gastric band surgery following maximum preoxygenation and rapid-sequence induction (RSI) of anesthesia.

Detailed Description

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Conditions

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General Surgery

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

HEALTH_SERVICES_RESEARCH

Blinding Strategy

SINGLE

Outcome Assessors
The person measuring and recording the study data ("timer") will be blinded.

Study Groups

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A - 25° head-up position

Participants will be positioned at a 25° head-up position for procedure.

Group Type ACTIVE_COMPARATOR

25° head-up position

Intervention Type OTHER

Angle person is positioned for procedure.

B - 55° head-up position

Participants will be positioned at a 55° head-up position for procedure.

Group Type ACTIVE_COMPARATOR

55° head-up position

Intervention Type OTHER

Angle person is positioned for procedure.

Interventions

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25° head-up position

Angle person is positioned for procedure.

Intervention Type OTHER

55° head-up position

Angle person is positioned for procedure.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* American Society of Anesthesiologists (ASA) physical status II-III patients
* Body Mass Index (BMI) of 40-60
* Scheduled for an elective laparoscopic adjustable gastric band surgery

Exclusion Criteria

* Patients with abnormalities of the upper airway that require awake tracheal intubation
* Asthma
* Chronic obstructive pulmonary disease
* Pregnant patients
Minimum Eligible Age

18 Years

Maximum Eligible Age

60 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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University of Kansas Medical Center

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Mirsad Dupanović, MD

Role: PRINCIPAL_INVESTIGATOR

University of Kansas Medical Center

Locations

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University of Kansas Medical Center

Kansas City, Kansas, United States

Site Status

Countries

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United States

Other Identifiers

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11506

Identifier Type: -

Identifier Source: org_study_id

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