Investigating the comparative of pain intensity due to intravenous injection of thiopental sodium, propofol, diazepam and etomidate during induction of general anesthesia

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

IRCT

Registry ID

IRCT20190822044581N2

Enrollment

200

Registered

2020-04-29

Start date

2020-06-21

Completion date

Unknown

Last updated

2020-05-18

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

Conditions

Pain.

Interventions

Intervention 1: First intervention group: Diazepam is given as a pre-medication at a dose of 0.1 mg / kg and with a volume of 5 cc intravenously and no medication is taken beforehand. Simultaneously w

Eligibility

Sex/Gender

All

Age

15 Years to 50 Years

Inclusion criteria

Inclusion criteria: Having general anesthesia based on pre-anesthesia examinations Age 15 to 50 years The surgery is optional 4 - having the risk of anesthesia I and II Do not have drug addiction Do not have mental and psychological disorders based on pre-anesthesia examinations Do not have diabetic disease Do not have systemic neurological disease

Exclusion criteria

Exclusion criteria: Non-cooperation of research units with researchers

Design outcomes

Primary

Measure	Time frame
Injection pain. Timepoint: Simultaneously with intravenous injection of the drug. Method of measurement: Pain measurement scale.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactNaeem Abdi

Yasouj University of Medical Sciences

abdi.naeim@yahoo.com+98 74 3222 3853

Outcome results

None listed

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