Selection of Laryngeal Mask Airway in Patients With Slender Somatotype

NCT ID: NCT02732613

Last Updated: 2016-04-08

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

UNKNOWN

Clinical Phase

NA

Total Enrollment

118 participants

Study Classification

INTERVENTIONAL

Study Start Date

2016-04-30

Study Completion Date

2016-11-30

Brief Summary

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The size selection of Laryngeal Mask Airway classic is usually followed the manufacturer's recommendation based on the patient's ideal weight. But sometimes the patient is tall and slim, the actual weight is much less than the ideal weight. This phenomenon might affect the success rate of insertion. Previous studies had demonstrated that the selection of Laryngeal Mask Airway size based on ideal weight could improve the success rate of insertion; therefore, this study was designed to prove whether this conclusion also applies to the tall and thin patients.

Detailed Description

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One hundred and eighteen patients adult patients,actual body weight much less than ideal body weight will be assigned randomly to two groups (Actual weight Group or Ideal weight Group). Size selection was guided by the recommendations of manufacturer, patients will be based on the actual body weight in Actual weight Group while ideal body weight in Ideal weight Group.

The success rate of first attempt,number of adjustments, insertion time, ease of insertion, overall success rate, oropharyngeal leak pressure and fiberoptic view will be recorded and compared. The occurrences of respiratory complications such as sore throat, hoarseness, and dysphonia will be observed and recorded.

Conditions

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Size of Laryngeal Mask Airway Body Weight Success Rate of First Attempt Complication

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Blinding Strategy

DOUBLE

Participants Investigators

Study Groups

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Actual weight Group

Patients in Actual weight Group: The selection of Laryngeal Mask Airway classic will be based on actual body weight, followed the recommendations of manufacturer (size 3 for weight \< 50 kg, size 4 for weight 50-70 kg, and size 5 for weight \> 70 kg ).

Group Type EXPERIMENTAL

Laryngeal Mask Airway

Intervention Type DEVICE

If there were any conflicts of the Laryngeal Mask Airway classic size selection in slim patients by the actual or ideal body weight, size selection will based on actual body weight in Actual weight Group while ideal body weight in Ideal weight Group.

Ideal weight Group

Patients in Ideal weight Group: The selection of Laryngeal Mask Airway classic will be based on ideal body weight, followed the recommendations of manufacturer ( size 3 for weight \< 50 kg, size 4 for weight 50-70 kg, and size 5 for weight \> 70 kg ).

Group Type EXPERIMENTAL

Laryngeal Mask Airway

Intervention Type DEVICE

If there were any conflicts of the Laryngeal Mask Airway classic size selection in slim patients by the actual or ideal body weight, size selection will based on actual body weight in Actual weight Group while ideal body weight in Ideal weight Group.

Interventions

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Laryngeal Mask Airway

If there were any conflicts of the Laryngeal Mask Airway classic size selection in slim patients by the actual or ideal body weight, size selection will based on actual body weight in Actual weight Group while ideal body weight in Ideal weight Group.

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

1. Adult Patients undergo elective surgery of American Society of Anesthesiologists (ASA) physical status 1-2, aged from 18 to 60;
2. Patients' actual weight much less than ideal weight.

Exclusion Criteria

1. Patients with gastroesophageal reflux disease;
2. Patients with predicted difficult airway;
3. Patients with preexisting airway diseases or significant upper airway infection.
Minimum Eligible Age

18 Years

Maximum Eligible Age

60 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Sun Yat-sen University

OTHER

Sponsor Role collaborator

XiQiang Huang

OTHER

Sponsor Role lead

Responsible Party

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XiQiang Huang

Attending doctor, Department of anesthesiology, Principal Investigator

Responsibility Role SPONSOR_INVESTIGATOR

Central Contacts

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Xiqiang Huang, Bachelor

Role: CONTACT

+86-18923324188

Yiquan Lin, Master

Role: CONTACT

+86-15915896526

Other Identifiers

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ZSPH20160303

Identifier Type: -

Identifier Source: org_study_id

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