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Comparing two different anaesthesia monitors for sevoflurane an anaesthetic gas usage-during general anaesthesia

“ Comparision of Adequacy of Anaesthesia(AoA) monitor with CONOX monitor in terms of consumption of sevoflurane during routine general anaesthesia’’ – A Randomised controlled trial.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2020/11/028864
Enrollment
90
Registered
2020-11-03
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: Z038- Encounter for observation for other suspected diseases and conditions ruled out

Interventions

Intervention1: Adequacy of Anaesthesia (AOA) monitor: This monitor will be used throughout the surgery i.e 3 to 5 hours Control Intervention1: Conox monitor: This monitor will be used throughout the s

Sponsors

Jawaharlal institute of postgraduate medical education and research
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients within 18 to 60 years of age, undergoing elective surgery for 3 to 5 hours under general anaesthesia with endotracheal tube, in JIPMER - Puducherry

Exclusion criteria

Exclusion criteria: 1)Patients receiving any form of regional anaesthesia 2) Laparoscopic surgeries

Design outcomes

Primary

MeasureTime frame
To compare the efficacy of both the monitoring systems AOA and CONOX interms of sevoflurane consumption.Timepoint: At the end of surgery i.e around 2 to 5 hours,amount of sevoflurane consumed will be calculated and compared between two groups.

Secondary

MeasureTime frame
1) To compare the amount of fentanyl used for surgeries lasting for 3 to 5 hours between the groups. 2)To find out incidence of intra operative awareness between the groups. 3) To compare the emergence timebetween the groups. Timepoint: At the end of surgery i.e 2 to 5 hours amount of fentanyl used will be calculated.Post operatively after 24 hours questionnaire will be given to find out intraoperative awareness.

Countries

India

Contacts

Public ContactArulkumaran R

Jawaharlal Institute Of Postgraduate Medical Education and Research

anushacherian@gmail.com

Outcome results

None listed

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