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Comparison between intravenous propofol (sleep inducing agent) and inhalation sevoflurane (sleep inducing agent) for ease of classic laryngeal mask airway insertion in patients undergoing elective surgery

A prospective randomized single blinded comparative study between intravenous propofol and inhalation sevoflurane for ease of classic laryngeal mask airway insertion in patients undergoing elective surgery

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2019/07/020357
Enrollment
80
Registered
2019-07-24
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: 8- Other Procedures

Interventions

Intervention1: Classic laryngeal airway insertion with 1% intravenous propofol: Patients will be randomly allocated into two groups (P and S) of 40 patients each. Group P will receive Propofol and gro

Sponsors

Midnapore Medical College
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. ASA PS I & II 2. Weight between 3. 30 kg to 70 kg 4. Surgeries where LMA can be used.

Exclusion criteria

Exclusion criteria: 1. Unwilling patients 2. ASA III & IV 3. Allergy to propofol 4. Oral surgeries 5. Heavy smokers (more than 20 cigarettes in a day) 6. Upper respiratory tract infection 7. Emergency surgeries. 8. Conditions where LMA insertion could not be done after four attempts.

Design outcomes

Primary

MeasureTime frame
Sevoflurane is as good an induction agent as propofol and it is advantageous for its hemodynamic stability is our expected outcome.Timepoint: August 2019 to July 2020

Secondary

MeasureTime frame
1.To observe the hemodynamic changes among two study groups. 2.Complications of LMA insertion. Timepoint: August 2019 to July 2020

Countries

India

Contacts

Public ContactPROSENJIT MUKHERJEE

Midnapore Medical College

docposhu@gmail.com9433727718

Outcome results

None listed

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