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Oropharyngeal leak pressure of LMA Protector Vs LMA Proseal in different head and neck positions

Comparison of oropharyngeal leak pressure of LMA Protector with ProSeal LMA in different head and neck positions

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/04/032611
Enrollment
70
Registered
2021-04-07
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: O- Medical and Surgical

Interventions

Intervention1: LMA Protector: oropharyngeal seal pressure of LMA Protector in neutral head position to extended and flexed head positions will be measured Control Intervention1: LMA Proseal: orophar

Sponsors

Maulana Azad Medical College and associated Lok Nayak Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Age >18 years ASA physical status I & II Anticipated duration of surgery

Exclusion criteria

Exclusion criteria: Known or predicted difficult airway -Patients with pre-existing cervical spine pathology (neck pain or tenderness in cervical spines or associated paraesthesia in upper limbs) -BMI > 35kg/m2 -Thorax, major upper abdomen, Head & neck surgeries -Surgeries requiring lateral or prone positioning -Patient at risk of aspiration such as pregnant patients, those with inadequate fasting, hiatal hernia, gastric outlet obstruction -Mouth opening less than 3 centimetres

Design outcomes

Primary

MeasureTime frame
oropharyngeal leak pressures of LMA protector and PLMA in different head and neck positionsTimepoint: after insertion of devices

Secondary

MeasureTime frame
ease of placement of devicesTimepoint: after placement of devices;ease of placement of nasogastric tubes through devicesTimepoint: after placement of devices;number of attempts for successful insertion of devicesTimepoint: after insertion of devices;postoperative sore throatTimepoint: 1, 2 and 24 hours after surgery;presence of blood on the cuff of devicesTimepoint: when the device is taken out from patients during extubation;time taken for successful insertion of devicesTimepoint: during insertion of devices

Countries

India

Contacts

Public ContactSUKHYANTI KERAI

Maulana Azad Medical College

drsukhi25@gmail.com09968527122

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026