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A study to find out the best propofol dose for producing loss of consciousness among different weight metrics.

A prospective observational study on correlation of induction dose of propofol according to different body weight metrics. - nil

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2024/09/073328
Enrollment
40
Registered
2024-09-04
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: -

Interventions

Control Intervention1: nil: nil

Sponsors

TRIHMS
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: ASA-PS I & II ROUTINE SURGERY CASE UNDER GENERAL ANAESTHESIA

Exclusion criteria

Exclusion criteria: UNCONTROLLED HYPERTENSION ISCHEMIC HEART DISEASE RENAL OR HEPATIC DYSFUNCTION SUSPECTED SUBSTANCE ABUSE.

Design outcomes

Primary

MeasureTime frame
To find out the best propofol induction dose among different body weight metrics.Timepoint: during induction—

Secondary

MeasureTime frame
Any serious adverse event.Timepoint: During induction period.—

Countries

India

Contacts

Public ContactDr Dusu Lalin

Tomo Riba Institute of Health and Medical Sciences.

drdusulalin@gmail.com7367967439

Outcome results

None listed

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