Multicenter Study of the Protector Laryngeal Mask

Airway Clinical Trial

Official title:

A Multicenter Study of the Protector Laryngeal Mask in Non Paralyzed, Anesthetized Patients

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03272776
• Other study ID #: MASKAPROTECTOR
• Status: Completed
• Start date: August 1, 2017
• Est. completion date: July 30, 2018

Study information

• Verified date: February 2019
• Source: Hospital General Universitario Gregorio Marañon
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

The study was designed to evaluate the success rate, time of insertion, sealing efficacy and security of the Protector Laryngeal Mask, a new second generation disposable supraglottic airway device, in patients undergoing elective surgery.

Description:

Laryngeal masks (LM) and supraglottic devices (SGD), in all their different forms, have become an authentic innovation in airway management especially in day surgery.

LMA Protector (Teleflex Medical, Athlone, Ireland) is a new disposable SGD currently available for anaesthetic practice. It is made of silicone (with no latex in its composition) and shares some of the characteristics of the second generation SGDs (as the presence of a gastric access channel); however, it has an additional drainage channel, both channels terminate distally in a camera behind the mask cuff. The presence of two drainage channels ("male" and "female") increases the patient safety against regurgitation, both of distal gastric content and secretions located in the oropharyngeal region. The gastric access channel called "female" also allows the insertion of a nasogastric tube if required. These drainage channels are useful for diagnosing the correct position of the mask, since the observation of leaks or gas through it can help diagnose a displacement the mask.

LMA Protector is designed with a preformed anatomic curve, and the airway conduct has an elliptical cross section, which ends distally in the mask. This design follows the anatomy of the human airway, which facilitates the insertion of the device. The softness of the mask material allows easy insertion.

Doubts regarding the transmission of infectious diseases with reusable devices makes disposable devices such as LMA Protector, one of the most interesting devices for use in anaesthetic procedures that are usually performed with SGD.

Its characteristics in the design, composition by a smooth and atraumatic material, the presence of two gastric drainage accesses, with potential improved patient safety and its characteristic of being disposable suggests a significant expansion of its use in the coming years .

In contrast to other SGDs that have been evaluated extensively, to date there are no large clinical studies showing its suitably and performance in a daily clinical scenario.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 280
• Est. completion date: July 30, 2018
• Est. primary completion date: July 30, 2018
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 75 Years

Eligibility

Inclusion Criteria:

• Surgery procedures usually performed with supraglottic devices.

• ASA physical status I-III patients

• Age 18-75

• Signed inform consent

Exclusion Criteria:

• Patients with known difficult airway

• Patients with predicted difficult airway

• Patients with increased risk of aspiration

• Patient refusal to participate in the study.

Related Conditions & MeSH terms

• Airway

Intervention

Device:
• Protector Laryngeal Mask airway
Evaluate the time of insertion, performance, security and insertion success rate of the Protector Laryngeal Mask in patients under general anasthesia.

Locations

Country	Name	City	State
Spain	Servicio de Anestesia, Hospital General Universitario Gregorio Marañon	Madrid

Sponsors (2)

Lead Sponsor	Collaborator
Matilde Zaballos	Teleflex

Country where clinical trial is conducted

Spain, 

References & Publications (4)

Brimacombe JR, editor. Laryngeal Mask Anesthesia. Principles and practice. 2nd Ed. Filadelfia. 2005.

Van Zundert AA, Skinner MW, Van Zundert TC, Luney SR, Pandit JJ. Value of knowing physical characteristics of the airway device before using it. Br J Anaesth. 2016 Jul;117(1):12-6. doi: 10.1093/bja/aew106. Epub 2016 May 4. — View Citation

Zaballos García M, López Álvarez S, Agustí Martínez-Marcos S, Blanco Sánchez T, Bustos Molina F, Cabré Fabré P, Cordero Lorenzo JM, Izquierdo Villaroya B, Lafuente Ojeda N, M. López Gil M, Rodríguez Archilla A, Zaballos Bustingorri J Recomendaciones prácticas de uso de la mascarilla laríngea en Cirugía Ambulatoria. Cir May Amb 2008; 13: (1) 4-26.

Zaballos García M, López Álvarez S, Agustí Martínez-Marcos S, Blanco Sánchez T, Bustos Molina F, Cabré Fabré P, et al. Nuevas aportaciones de la mascarilla laríngea en cirugía ambulatoria. Contribución de la mascarilla laríngea Supreme. Cir May Amb 2011; 16(2): 60-6.

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Evaluate the number of attempts to insert of the LMA Protector	Insertion attempts: from picking up the LMA Protector until the mask is placed into the patient mouth . (in numbers)	The number of insertion attempts will be collected after anesthesia induction: 1 minute after the administration of propofol
Secondary	Blood pressure during insertion of LMA protect	Blood pressure in mmHg	Baseline and every 3 minutes until 6 minutes after insertion of the LMA protector
Secondary	Heart rate during insertion of LMA protect	heart rate in beep per minute	Baseline and every 3 minutes until 6 minutes after insertion of the LMA protector
Secondary	BIS data	number from 100 (awake) to 40-45 (anesthetic status)	Baseline and every 3 minutes until 6 minutes after insertion of the LMA protector (To evaluate the evolution of BIS values during insertion of the LMA
Secondary	Oropharyngeal leak pressure of the LMA Protector	The Oropharyngeal leak pressure of the LMA Protector will be determined with an intracuff pressure of 60 cm H2O by closing the expiratory valve of the breathing circle circuit at a fixed gas flow of 3 L/min and noting the pressure at which an oropharyngeal leak occurs. (in cm H2O)	The Oropharyngeal leak pressure of the LMA Protector will be collected 5 minutes after the LMA Protector will be inserted

External Links

•   Teleflex® LMA® Protector™ Airway