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A Study Comparing Two Anesthetic Drugs, Propofol and Sevoflurane, for Inserting a Breathing Mask in Children

A Prospective Randomized Comparative Study of Induction with Propofol versus Sevoflurane for Laryngel Mask Airway in Children. - Nil

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/02/104019
Enrollment
70
Registered
2026-02-16
Start date
Unknown
Completion date
Unknown
Last updated
2026-03-02

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

Conditions

Health Condition 1: K409- Unilateral inguinal hernia, without obstruction or gangrene Health Condition 2: N430- Encysted hydrocele Health Condition 3: N471- Phimosis Health Condition 4: O- Medical and Surgical Health Condition 5: K353- Acute appendicitis with localizedperitonitis

Interventions

Intervention1: Laryngeal Mask airway: Laryngeal Mask Airway according to age and weight of the child will be used after Induction with injection propofol or inhalational agent sevoflurane. Control Int

Sponsors

Pacific Medical College and Hospital, Udaipur
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: American Society of Anesthesia Grade 1 and 2. Schedule for minor Elective surgery under General Anesthesia requiring Laryngeal Mask Airway insertion. Obtained Informed consent from Parents or Legal Guardian.

Exclusion criteria

Exclusion criteria: Refusal of consent. Known or suspected difficult Airway. Upper respiratory tract infection within thebpast 2 weeks. Known allergy to Propofol, sevoflurane or Laryngeal Mask Airway components. Neurological or neuromuscular disorders, severe cardiopulmonary diseases. Oropharyngeal pathology. At risk of aspiration.

Design outcomes

Primary

MeasureTime frame
Compare time and attempts for Laryngeal Mask Airway insertion.Timepoint: Vital parameters will be recorded at baseline,at Induction, after insertion of Laryngeal Mask Airway at 2 minutes, 5 minutes, 10 minutes and then every 15 minutes till complete recovery from Anaesthesia.

Secondary

MeasureTime frame
Assess hemodynamic changes. Eg Heart rate, Blood Pressure, spO2.Timepoint: Will be assessed at Baseline , 2 minutes, 5 minutes, 10 minutes, 15 minutes then every 15 minutes till complete recovery from anaesthesia.

Countries

India

Contacts

Public ContactDr Ramakant

Pacific Medical College and Hospital, Udaipur

dr.rkbhul@gmail.com8058021697

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Mar 14, 2026