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Respiratory adverse events after removal of laryngeal airway device in children undergoing inguinal hernia repair with propofol versus sevoflurane

Respiratory adverse events after removal of laryngeal airway device (LMA) in children undergoing inguinal hernia repair under anaesthesia with propofol versus sevoflurane- A Comparative Randomised Open Label Study - NIL

Status
Active, not recruiting
Phases
Phase 3Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/09/073933
Enrollment
150
Registered
2024-09-13
Start date
Unknown
Completion date
Unknown
Last updated
2024-09-16

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

Conditions

Health Condition 1: - Health Condition 2: Z409- Encounter for prophylactic surgery, unspecified

Interventions

Intervention1: Respiratory adverse events comparison: Respiratory Adverse Events After LMA® Mask Removal in Children: A Randomized Trial Comparing Propofol to Sevoflurane Control Intervention1: Propof

Sponsors

Maharana Bhopal Government Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Consenting ASA PS 1-2 patients scheduled to undergo inguinal hernia repair presenting at our hospital will be included in the study

Exclusion criteria

Exclusion criteria: Patient allergic to study drug,patient had an acute exacerbation of asthma, upper respiratory tract infection,congenial heart disease, neurological disorders,full stomach,hiatus hernia,known or predicted difficult airway,facial or airway malformation, major abdominal and thoracic surgery,inability to swallow solid bolus of food

Design outcomes

Primary

MeasureTime frame
Respiratory adverse outcomesTimepoint: No. Of episodes

Secondary

MeasureTime frame
Quality of anaesthesia at the time of lma insertion, Hemodynamic parameters Emergence from anaesthesiaTimepoint: Upto 24 hrs postoperatively

Countries

India

Contacts

Public ContactDr Anita

Government medical College

Vbedimd@gmail.com9829025373

Outcome results

None listed

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