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Comparison of Laryngeal Mask Airway (LMA®) and Tracheal Tube in Modified Radical Mastectomy on Breast Cancer

Comparison of Laryngeal Mask Airway (LMA®) and Tracheal Tube for Airway Management in Modified Radical Mastectomy on Breast Cancer

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00638599
Acronym
LMATBBC
Enrollment
200
Registered
2008-03-19
Start date
2008-01-31
Completion date
2009-07-31
Last updated
2009-07-15

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

Conditions

Breast Cancer

Keywords

Intubation, intratracheal, Homeostasis, Mastectomy, modified radical, Breast Neoplasms

Brief summary

Airway management in anesthesia is critical to guarantee appropriate treatment of possible respiratory complications and successful operative practice. LMA® is an alternative to tracheal tube in some surgeries like as mastectomy on breast cancer. Given no need using muscular relaxants in mastectomy, the investigators hypothesized that LMA® would be a superior manner in airway management in radical modified mastectomy on breast cancer than the tracheal tube, and the LMA® might produce less influence on patients' circulatory homeostasis, and easier to be placed before operation.

Interventions

DEVICELMA®

LMA® is placed after anesthesia induction and removed after the operation

DEVICEEndotracheal tube

Standard endotracheal tube is inserted after anesthesia induction and extubated after the operation

Sponsors

Nanjing Medical University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

* Chinese * Diagnosed breast cancer * Undergoing modified radical mastectomy * Agreed to participate the study with informed contract.

Exclusion criteria

* Organic dysfunction * Long-lasting post-anesthetic care unit(PACU) staying.

Design outcomes

Primary

MeasureTime frame
Circulatory Homeostasis15min prior to operation to 15min posterior to operation

Secondary

MeasureTime frame
Airway pressure15min prior to operation to 15min posterior to operation
Blood gas15min prior to operation to 15min posterior to operation
Airway complicationsStart of operation to 6h after operation

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026