Assessment Of Hemodinamic Effect Of Propofol

Phase 2

Completed

• Conditions: Propofol adverse events.; Other and unspecified general anaesthetics; Y 48.2

• Registration Number: IRCT2013093014831N1
• Lead Sponsor: Ahvaz Jundishapour University Of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 22 February 2018

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 58

Inclusion Criteria

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

Exclusion Criteria

Not provided

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
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 Outcome Measures

Name	Time	Method
Vomiting and Nausea. Timepoint: at end surjery. Method of measurement: Observation.