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Fentofol vs. Ketofol for painful procedures in the emergency department

Comparison of Fentofol with Ketofol to achieve the Aldret score of 12 in painful procedures in the emergency department

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016050615941N4
Enrollment
192
Registered
2017-09-11
Start date
2017-10-01
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Painful procedures in the emergency department.

Interventions

Intervention 1: Arm 1: Intervention name: Fentofol (Fentanyl+ Propofol) Intervention description: Fentanyl (1 microgram/Kg by slow intravenous injection) and Propofol ( 1 milligram/Kg by slow intraven
Treatment - Drugs
Arm 1: Intervention name: Fentofol (Fentanyl+ Propofol) Intervention description: Fentanyl (1 microgram/Kg by slow intravenous injection) and Propofol ( 1 milligram/Kg by slow intravenous injection)
Arm 2: Intervention name: Ketofol (Ketamine+ Propofol) Intervention description: Ketamine (1milligram/Kg by slow intravenous injection) and Propofol ( 1 milligram/Kg by slow intravenous injection) ar

Sponsors

Shahrad Tajaddini (investigator)
Lead Sponsor

Eligibility

Sex/Gender
All
Age
16 Years to 75 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: all patients over 16 years of age for whom a painful procedure needs to be performed in the emergency department. Exclusion criteria: presence of any co-morbidity (ASA score more than 1); procedure needs to be done in the operating room; Spo2 less than 92%; systolic blood pressure less than 100mmg; GCS (Glasgow coma scale) score less than 15; patient refusal to participate

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Time to achieve the Aldret score of 12. Timepoint: after the procedure ended. Method of measurement: counting minutes after the beginning of drug administration.

Secondary

MeasureTime frame
Adverse reactions. Timepoint: during and after the procedure. Method of measurement: recording any adverse reactions attributable to the drugs.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAmirhossein Mirafzal

Kerman University of Medical Sciences

a.mirafzal@yahoo.com- mirafzal@kmu.ac.ir+98 34 3223 5011

Outcome results

None listed

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