Assessment Of Hemodinamic Effect Of Propofol

Assessment Of Hemodynamic Effect Of Different Infusion Rates Of Propofol In Surjery Patient In Ahvaz Emam KHomini Hospital

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

IRCT

Registry ID

IRCT2013093014831N1

Enrollment

Registered

2013-11-12

Start date

2012-12-20

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

Propofol adverse events. Other and unspecified general anaesthetics

Interventions

Intervention 1: After benig anesthetically induced in group A have been infusion propofol with dose 50ug/kg/min and group B with dose100ug/kg/min and it stops 15 minutes before the termination of the

Treatment - Drugs

After benig anesthetically induced in group A have been infusion propofol with dose 50ug/kg/min and group B with dose100ug/kg/min and it stops 15 minutes before the termination of the operation

Group B: Infusion of propofol with dose 100ug/kg/min and it stops 15 minutes before the termination of the operation

Eligibility

Sex/Gender

All

Age

15 Years to 55 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria:ASAclass-1?age between15-55 years. Exclusion criteria:ASAclass>2?Addiction;liver,kidney,cardiac disease?sensivity for egg?Hemodinamic unstability

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

Measure	Time frame
Blood Pressure. Timepoint: at minutes 0-2-5-10-15-20-30-45-60. Method of measurement: Milimeter-Mercury(mmHg)by Automatic pressure gauge.	—

Secondary

Measure	Time frame
Vomiting and Nausea. Timepoint: at end surjery. Method of measurement: Observation.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSHoleh Nesioonpour

Ahvaz jundishapour University Of Medical Sciences

nesioonpour.sh@ajums.ac.ir+98 61 1222 0168

Outcome results

None listed

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