A clinical trial comparing the efficacy of two Supraglottic Airway Devices ie the Baska Mask versus the Proseal Laryngeal Mask Airway in patients undergoing elective surgeries under general anesthesia

Efficacy of Baska Mask versus Proseal Laryngeal Mask Airway in elective surgeries under general anesthesia - a Randomized Controlled Trial - NIL

Status

Active, not recruiting

Phases

Phase 2Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2024/07/071669

Enrollment

Registered

2024-07-31

Start date

Unknown

Completion date

Unknown

Last updated

2024-08-19

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

Conditions

Health Condition 1: 8- Other Procedures

Interventions

Intervention1: Supraglottic Airway Device (SAD): In Group A Proseal Laryngeal Mask Airway (PLMA) will be inserted and time taken for insertion,ease of insertion and number of attempts for insertion wi

Eligibility

Inclusion criteria

Inclusion criteria: Patients of either gender, from 18 to 60 years of age, belonging to the American Society of Anesthesiologists (ASA) classes I, II and III.

Exclusion criteria

Exclusion criteria: Patients refusal, BMI more than or equal to 30 kg per metre square, Restricted mouth opening, Surgeries lasting more than 2 hours, Burns and swelling in neck, High aspiration risk with poor pulmonary compliance

Design outcomes

Primary

Measure	Time frame
To measure time taken for insertion, ease of insertion and number of attempts for insertion between the Proseal Laryngeal Mask Airway and the Baska MaskTimepoint: At start of insertion of both devices	—

Secondary

Measure	Time frame
To measure oropharyngeal seal pressure (OSP) logged at two different times and post- insertion complications between Baska Mask and Proseal Laryngeal Mask Airway Timepoint: 5 minutes and 15 minutes	—

Countries

India

Contacts

Public ContactDr R Ajisha Rachel

Sri Venkateshwaraa Medical College Hospital and Research Centre

drkrishnaprabu@gmail.com9943770977

Outcome results

None listed

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