effect of intervenous administration of dexametason and fentanil on reduction of propofol induced pain during intravenous injection

comparision of effect of intervenous administration of dexametason with fentanil on reduction of propofol induced pain during intravenous injection

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT2015021015281N2

Enrollment

150

Registered

2015-11-04

Start date

2015-02-20

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

Complications of anaesthesia. Other complications of anaesthesia

Interventions

Intervention 1: Control group: first group, 5 cc normal salin 0.9 , 1 min before propofol injection. Intervention 2: Interventional group: second group, 8 mg dexametason, 5 cc , 1 min before propofol

Treatment - Drugs

Control group: first group, 5 cc normal salin 0.9 , 1 min before propofol injection

Interventional group: second group, 8 mg dexametason, 5 cc , 1 min before propofol injection

Interventional group: thirth group,100 micro gram fantanil, 5 cc , 1 min before propofol injection

Eligibility

Sex/Gender

All

Age

16 Years to 60 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Patients of 16 to 60 y/o admitted for general surgery Exclusion criteria: the patients who received sedative drugs 48hr before operation; have drug allergy; with neurological disorders or mental,drug Addicts; Pregnant women and who require a rapid induction of anesthesia

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

Measure	Time frame
Effect of fentanil on reduction of propofol induced pain during intravenousinjection. Timepoint: 1 minute after injection of propofol. Method of measurement: Fill questionare and visual scale.;Effect of dexametason on reduction of propofol induced pain during intravenousinjection. Timepoint: 1 minute after injection of propofol. Method of measurement: Fill questionare and visual scale.	—

Secondary

Measure	Time frame
Dermal side effects. Timepoint: From injection time untii ending of recovery time. Method of measurement: Fill questionare.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDR Seyedebrahim Sadeghi

Shiraz University of Medical Sciences

esadeghi@sums.ac.ir+98 71 4333 3278

Outcome results

None listed

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