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A comparative study of two inhalational anaesthetic agent for patients undergoing surgery in general anaesthesia.

A randomized controlled study of haemodynamic parameters, recovery characteristics of desflurane and sevoflurane in adult patients receiving BIS guided general anaesthesia

Status
Active, not recruiting
Phases
Phase 3Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/05/067245
Enrollment
80
Registered
2024-05-13
Start date
Unknown
Completion date
Unknown
Last updated
2024-05-27

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

Conditions

Health Condition 1: O- Medical and Surgical

Interventions

Intervention1: Desflurane: The dose of the desflurane will be Bispectral index guided and the BIS score will be maintained between 60 to 40, used during maintenance of anaesthesia, route of administ

Sponsors

Dr Varun B R
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.ASA grade I and grade II Patients 2.Age- 18 to 65 years of either sex 3.Patients undergoing elective surgeries under general anaesthesia

Exclusion criteria

Exclusion criteria: 1.Patient refusal, 2.Pregnancy, 3.significant cardiopulmonary diseases, hepatic and renal dysfunction, 4.chronic alcohol or narcotic drug abuse, 5.Known allergy or hypersensitivity to study drugs.

Design outcomes

Primary

MeasureTime frame
1.Time for early recovery characteristics. 2.Time for intermediate recovery characteristics. Timepoint: 1.from the time of discontinuation of anaesthesia 2.5min, 10min, 15min in post anaesthesia recovery room

Secondary

MeasureTime frame
1.Haemodynamic changes if any viz. Heart Rate, Mean Arterial Pressure, Systolic Blood Pressure, Diastolic Blood Pressure. Timepoint: 1. baseline,2min,3min,4min,5min,10min,15min,20min,30min,40min,50min,60min

Countries

India

Contacts

Public ContactDr Yogesh Kumar Manik

Lala Lajpat Rai Memorial Medical college

dr.yogeshkmanik@gmail.com9634857368

Outcome results

None listed

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