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Comparision of quantitative use of sevoflurane with high initial concentration Vs incremental induction technique

Comparision of quantitative use of sevoflurane with high initial concentration Vs incremental induction technique in children at a tertiary care centre - Nil

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/02/063181
Enrollment
70
Registered
2024-02-27
Start date
Unknown
Completion date
Unknown
Last updated
2024-03-04

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

Conditions

Health Condition 1: 4- Measurement and Monitoring

Interventions

Intervention1: 8% Sevoflurane: One group is induced for Anaesthesia using 8% of the inhalation agent Sevoflurane. Control Intervention1: 8% Sevoflurane: One group is induced for Anaesthesia using 8% o

Sponsors

Sri Ramachandra Institute of Higher Education and Research
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Children between the age group of 1 to 12 posted for elective surgeries.

Exclusion criteria

Exclusion criteria: Known history of allergies to inhalation agents Any contraindications to inhalation induction Emergency surgery

Design outcomes

Primary

MeasureTime frame
Quantity of inhalation agent requirementTimepoint: Quantity of inhalation agent consumption measured at the end of induction of anesthesia—

Secondary

MeasureTime frame
Time taken for ease of IV cannulation Hemadynamics parametersTimepoint: Every 2 minutes during induction—

Countries

India

Contacts

Public ContactMADHURI G P

Sri Ramachandra Institute of Higher Education and Research

venkymail2014@gmail.com9871547993

Outcome results

None listed

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