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A study to compare and determine the best time to insert tube over the breathing passage after starting anaesthesia with propofol medicine in patients undergoing surgery

A Randomised Controlled Study to Determine the Appropriate Time for Placement of LMA R SupremeTM Supraglottic Airway Device with Propofol Induction. - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/04/109429
Enrollment
320
Registered
2026-04-27
Start date
Unknown
Completion date
Unknown
Last updated
2026-06-01

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 Health Condition 2: C00-D49- Neoplasms

Interventions

Intervention1: LMA insertion after induction with propofol: To determine the appropriate time for LMA insertion after induction of anaesthesia with propofol Control Intervention1: Comparison of differ

Sponsors

Tata Memorial Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Adult patients more than or equal to18 years of age with an American Society of Anaesthesiologists ASA I - III scheduled for elective surgeries under general anaesthesia for which LMA is an appropriate choice for airway management

Exclusion criteria

Exclusion criteria: 1. Patient refusal to participate 2. Patient at risk of aspiration like patients who are inadequately fasting, patients with intestinal obstruction/perforation. 3. Patients undergoing emergency surgery 4. Patient with restricted mouth opening 5. Patients with upper airway obstructions such as airway tumor, abscess, edema and/or hematoma 6. Patient with disrupted upper airway, facial or upper airway trauma, airway burns 7. Patients who are morbidly obese(BMI more than 40kg/m ) 8. Pregnant patients 9. Patients with poor lung compliance 10. Patients in whom iv Propofol is to be avoided

Design outcomes

Primary

MeasureTime frame
Determine the appropriate time for LMA SupremeTM supraglottic airway device insertion after induction of anaesthesia with IV Propofol.Timepoint: 30/60/90 seconds after induction with propofol as per the group allocated to the patient

Secondary

MeasureTime frame
1. Determine the incidence of improper placement of LMA at all the three time intervals. 2. Determine the extent of adverse response to airway manipulation like coughing, gagging, laryngospasm and patient movements at all the three time intervals of LMA insertion.Timepoint: 30/60/90 seconds after induction with propofol as per the group allocated to the patient

Countries

India

Contacts

Public ContactSmarasmita Sen

ACTREC

bhaktiamit@gmail.com02227405000

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Jun 11, 2026