Skip to content

A study to compare between two devices that allows delivering oxygen to the patient during a surgical procedure.

Comparison of Laryngeal Mask Airway Protector and Intubating Laryngeal Mask Airway for Ease of Fiberoptic-Guided Tracheal Intubation in Adult Patients: A One-Year Hospital-Based Randomized Control Trial - NIL

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/01/079241
Enrollment
68
Registered
2025-01-22
Start date
Unknown
Completion date
Unknown
Last updated
2025-02-03

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

Conditions

Health Condition 1: K358- Other and unspecified acute appendicitis

Interventions

Intervention1: Intubating LMA: After induction of general anaesthesia, intubating LMA of size #3 or #4 will be inserted depending on the weight of the patient and checked for bilateral air entry. Afte

Sponsors

Dr Kevin Santosh Joseph
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: ASA status I, II, III Patients undergoing elective surgery under general anaesthesia Patients willing to give consent

Exclusion criteria

Exclusion criteria: Patients undergoing emergency surgeries Patients not willing to give consent Patients with pharyngeal pathology Patients having anatomical deformity of mouth, pharynx and larynx Patients with high risk for aspiration Patients with high airway resistance (severe obesity) Pregnant patients

Design outcomes

Primary

MeasureTime frame
To compare the ease for fibreoptic-guided tracheal intubation through the Intubating LMA with the LMA Protector.Timepoint: 0 minutes, (Intraoperative)

Secondary

MeasureTime frame
To evaluate the position of the LMA Protector and Intubating LMA with respect to the glottic aperture.Timepoint: 0 minutes, (Intraoperative)

Countries

India

Contacts

Public ContactDr. Rajesh Mane

KLE DR Prabhakar Kores hospital

drrajeshmane@gmail.com9844131062

Outcome results

None listed

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