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Comparision of two different methods for determining the depth of anesthesia during the initial phase of anesthesia in patients undergoing surgery under general anaesthesia.

Comparison of Bispectral Index (BIS)-guided vs Clinically guided propofol induction in Adult Patients undergoing Elective Surgery under General Anaesthesia: A Prospective Randomised Clinical Trial - nil

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/08/093142
Enrollment
50
Registered
2025-08-18
Start date
Unknown
Completion date
Unknown
Last updated
2025-09-15

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

Conditions

None listed

Interventions

Intervention1: Propofol infusion by Bispectral index.: In OT, Baseline parameters NIBP, HR, ECG, SpO2 noted Preoxygenation by 100% O2 followed by IV Fentanyl 2 mcg/kg 1) Group C ? This group of partic

Sponsors

Prameela
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patient ready to give informed written consent Men and women aged 18 years and older ASA physical status class I to III Patient coming for elective surgery under general anaesthesia

Exclusion criteria

Exclusion criteria: Pregnant female Lactating mother Baseline BP and/or HR fall greater than 20% on induction Emergency surgeries

Design outcomes

Primary

MeasureTime frame
To evaluate and compare the effectiveness of BIS guided vs clinical guided anaesthesia induction by measuring propofol requirement Timepoint: Induction time—

Secondary

MeasureTime frame
To evaluate the safety profile of BIS guided vs clinical guided anaesthesia induction by measuring hemodynamic parametersTimepoint: Induction time—

Countries

India

Contacts

Public ContactDr Sumit Bansal

AIIMS Rajkot

sumitbansal05@gmail.com9968720446

Outcome results

None listed

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