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Comparison between two types of Laryngeal mask airways in terms of the development of sore throat after its use

Comparison of incidence of sore throat with laryngeal mask airway protector and laryngeal mask airway proseal: A randomized clinical trial.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/08/044587
Enrollment
118
Registered
2022-08-03
Start date
Unknown
Completion date
Unknown
Last updated
2022-10-17

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

Conditions

Health Condition 1: R50-R69- General symptoms and signs

Interventions

Intervention1: LMA PROTECTOR: In this group, LMA PROTECTOR will be used for securing airway under general anaesthesia and patient will be followed up for sore throat and other related symptoms Control

Sponsors

Jawaharlal Institute of Post graduate Medical Education and Research
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: ASA 1and 2 patients Elective surgery under general anaesthesia lasting upto 2 hours.

Exclusion criteria

Exclusion criteria: Pregnant woman Patients undergoing emergency surgery Patients at risk of aspiration Patients with history of sorethroat or URI upto 2 weeks prior to surgery

Design outcomes

Primary

MeasureTime frame
To compare the incidence of sore throat between LMA Protector and LMA ProsealTimepoint: At 1 hour, 6 hours, 24 hours—

Secondary

MeasureTime frame
To compare the device insertion time, success at first attempt insertion rates and ease of insertion in each device. To compare the oropharyngeal seal pressure in each device. To compare the ventilator parameters with each device To compare the incidence of dysphagia, dysphonia, hoarseness of voice in each device.Timepoint: At 1 hour, 6 hours, 24 hours—

Countries

India

Contacts

Public ContactDr Vidya Mohan

Jawaharlal Institute of Postgraduate Medical Education and Research

priyaab8@gmail.com8903468132

Outcome results

None listed

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